# Petition for Writ of Certiorari — Campbell v. United States

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## Record

- **Collection:** Supreme Court brief
- **Document type:** Petition for Writ of Certiorari
- **Published:** January 1, 2002
- **Citation:** 537 U.S. 950

## Text

FILED

') 02 894 apr 252004

OFFICE OF THE CLERK

IN THE
SUPREME COURT OF THE UNITED STATES

RODERICK ALAN CAMPBELL
Petitioner

UNITED STATES OF AMERICA
Respondent

PETITION FOR WRIT OF CERTIORARI TO
THE UNITED STATES COURT OF APPEALS
FOR THE FIRST CIRCUIT

Roderick A. Campbell, Pro Se
F.C.I. Fort Dix

P.O. Box 2000

Fort Dix, New Jersey 08640

I.

IT.

III.

QUESTIONS PRESENTED FOR REVIEW

WHETHER, CERTIORARI SHOULD BE GRANTED TO
RESOLVE A QUESTION- OF THE EVALUATION OF
WHETHER SCIENTIFIC EVIDENCE IS EXCULPATORY
UNDER THE STANDARD OF BRADY V. MARYLAND FOR
THE DEPTH OF UNDERSTANDING CHARGEABLE TO
THE DEFENSE, THE TRUTHFULNESS OF THE
GOVERNMENT DESCRIPTION OF THE DATA, AND THE
MINIMUM COMPETENCE REQUIRED OF THE REVIEW-
ING COURT?

WHETHER, CERTIORARI SHOULD BE GRANTED TO
DECIDE WHETHER THE UNITED STATES SENTENCING
GUIDELINES ARE STATUTORY LAW IN FACT AND
LAW WHICH MUST BE CHARGED AND PROVEN AS
AGGRAVATED OFFENSES RATHER THAN
CHARACTERISTICS OF THE OFFENSE?

WHETHER, CERTIORARI SHOULD BE GRANTED TO
DECIDE WHETHER THE PETITIONER’S SCIENTIFIC
EVALUATION OF NEWLY DISCOVERED ANALYTICAL
DATA NOT PRODUCED FOR TRIAL DEMONSTRATED A
COLORABLE PROOF OF ACTUAL INNOCENCE, SUCH
THAT ALL PROCEDURAL DEFECTS SHOULD BE
WAIVED AND THE CASE HEARD ON THE MERITS?

PARTIES

The parties of interest are all named on the cover of the Petition.

li

TABLE OF CONTENTS

QUESTIONS PRESENTED FOR REVIEW

TABLE OF CONTENTS

TRAVEL BELOW

TABLE OF AUTHORITIES

BACKGROUND FACTS

ARGUMENT:

I. CERTIORARI SHOULD BE GRANTED TO
RESOLVE THE EVALUATION OF SCIENTIFIC
EXCULPATORY EVIDENCE UNDER BRADY
V. MARYLAND:

II. © CERTIORARI SHOULD BE GRANTED TO
ESTABLISH THE STATUS OF THE UNITED
STATES SENTENCING GUIDELINES AS
STATING ELEMENTS OF A DRUG OFFENSE:

III. CERTIORARI SHOULD BE GRANTED TO
DECIDE WHETHER THIS PETITIONER’S
SCIENTIFIC EVIDENCE CONSTITUTES A
COLORABLE PROOF OF ACTUAL
INNOCENCE WARRANTING A FULL
EVIDENTIARY HEARING:

CONCLUSION

APPENDICES: A through N

iil

ill

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iV

Vill

23

29

TABLE OF AUTHORITIES °

Apprendi v. New Jersey, 530 U.S. 466 (2000) ..... 15, 16, 19, 22
Brady v. Maryland, 373 U.S. 83 (1963) .............-.. 10, 30
Leko v. Portuondo, 257 F.3d 89 (2"4 Cir. 2001) ............. 11
Daubert v. Merrill Dow Pharmaceuticals, Inc., 509 U.S. 579
8 Pe ee Cy eer re re ee ee nye Pre Tere 6, 10
Cae Bs PR, He SP EOP EROEND vids ki scencnvassonseawh 14
Harris v. Nelson, 394 U.S. 286 (1969) ...............-.00. 24
Herrera v. Collins, 506 U.S. 390 (1993) .................. 24
In re Grand Jury Application, 617 F.Supp. 199

SAAD: RUE Sha bi eee Cee chek old ueceoraviar pecans ns 5
Jones v. United States, 526 U.S. 227 (1999) ................ 15
Kinder v. United States, 119 L.Ed.2d 214 (1992) ........... 16
Marbury v. Madison, 5 U.S. 137 (1803) .................. 23
McClesky v. Zant, 499 U.S. 467 (1991) ................. 23, 29
McMillan v. Pennsylvania, 477 U.S. 79 (1986) .......... 16, 19
Miller v. Florida, 482 U.S. 423 (1987) ..................... 21
Miller v. United States, 564 F.2d 13 (1st Cir. 1977) ........... 13
Mullaney v. Wilbur, 421 U.S. 684 (1975) .................. 20
Murray v. Carrier, 477 U.S. 478 (1986) ............. 24, 25, 26
Passos-Paternina v. United States, 12 F.Supp.2d

121 (D.P.R. 1998), aff'd, 201 F.3d 428 (1st Cir. 1998) ......... 10
Phoenix v. Matesanz, 189 F.3d 20 (Ist Cir. 1999) ........... 11
R.L.C. v. United States, 503 U.S. 297 (1992) ............ 21, 22
Sanders v. United States, 373 U.S. 1 (1963) ................ 29
Saville v. United States, 451 F.2d 649

Re BEE bap bS en sae cen db Rado t a ch esows kabus ewan 29
Sawyer v. Whitley, 505 U.S. 333 (1991) ................ 24, 25

iV

Schlup v. Delo, 513 U.S. 298 (1995) ................ 24, 28, 29

Siciliano v. Voes, 834 F.2d 29 (1st Cir. 1987) ............... 13
United States v. Acosta, 963 F.2d 551 (2"4 Cir.1992) ........ i7
United States v. Beler, 20 F.3d 1428 (7% Cir. 1994) .......... 19
United States v. Boylan, 5 F.Supp.2d 274

ee Ter eo ee ie it en me 20
United States v. Butt, 731 F.2d 75 (1st Cir. 1984) ............ 13
United States v. Campbell, 61 F.3d 976

GP EU So b a'vne cen ee wens hak soe cea ae a 1, 33
United States v. Coleman, 188 F.3d 354

a Ee Eee ee eee PR pe 23
United States v. Cotton, 261 F.3d 397 (4t Cir.

2001), cert. granted, 122 S.Ct. 803 (2001) .................. 21
United States v. Edwards, 154 F.3d 915

yt SU 0 43:53 wha dee ea oa ee 11
United States v. Fields, 466 F.2d 119

(2 Cy. TIVE) GE PE DOO Cee) obs bois ce ecckks Goons 11
United States v. Garza-Juarez, 992 F.2d 896

eS ere Prey rr tre Fy Neen Pea ee We yy 13
United States v. Gonzalez, 259 F.3d 355

Go as SD sno ooh. k vceenans Mee oeener ee eeee ea 21
United States v. Jenning, 945 F.2d 129

Ga BOWED 0h b Nk bk tue eas ee werseeeeeaa eats 17
United States v. Johnson, 999 F.2d 1192

Phe SUED bi cakeaeneeuecelcadi ese oeee ae eee 17
United States v. Levay, 76 F.3d 671 (5th Cir. 1996) .......... 17
United States v. Nash, 64 F.3d 504 (9% Cir. 1996) ........... 29
United States v. Navarro, 145 F.3d 580 (34 Cir. 1998) ....... 29
United States v. Ramirez, 242 F.3d 348 (6 Cir. 2001) ....... 16

United States v. Richards, 67 F.3d 1531

ge 2 Tr eye ry rere ree 17
United States v. Robbins, 967 F.2d 1387

ae | EP rere r er Teer ee rT eae. 17
United States v. Rodriguez, 975 F.2d 999

rR: ROMER :0 ce sus pone 20 eves ee nek as Wek b eee ce anes 17
United States v. Roland-Gabriele, 938 F.2d 1231

LS gag Se See Pp beeen de eae ea ey eer Cey Fee 17
United States v. Salerno, 481 U.S. 739 (1987) .............. 18
United States v. Sanquist, 125 F.3d 573

Ejeet Gs BT ep ry erp apse ee nid Bo ey apy tig 2 py 11
United States v. Sciverner, 167 F.3d 525

FoR: ROPE 0440s coh sb eebaceun eateries Vieira 29

United States v. Thomas, 204 F.3d 381 (24 Cir. 2000),
rev'd in part, United States v. Thomas, 274 F.3d

og ee yee Fee re Sere ere rare yey we 20
United States v. Tran, 234 F.3d 798 (2"4 Cir. 2000) .......... 20
United States v. Underwood, 577 F.2d 157

ee Sy PEE Te res ee ee red ery eI eye ES PE ee 13
Williams v. United States, 503 U.S. 193 (1992) ............. 20

vi

PETITION FOR WRIT OF CERTIRARI

Petitioner, Roderick A. Campbell, Pro Se, respectfully
prays for the grant of a writ of certiorari to review the denial of
his request for a certificate of appealability in the United States
Court of Appeals for the First Circuit, entered as a final
judgment on November 26, 2001.

TRAVEL BELOW

The underlying criminal case has been reported as United
States v. Campbell, 61 F.3d 976 (1st Cir. 1995), cert. denied, 517 U.S.
1161 (1996). The matter for which the Petitioner sought a
certificate of appealability in the First Circuit Court of Appeals
was his Motion To Vacate, Set Aside, Or Correct Sentence,
Campbell v. United States, 97-CV-0274 (D.R.I.). The denial of
that Motion is reproduced in Appendix A.

The certificate of appealability requested in the Court of
Appeals was denied on September 6, 2001. See Appendix B.
The Appellate Court construed a timely Motion For
Withdrawal Of Decision as a motion for reconsideration, and
denied the same on November 26. See Appendix C.

This Court has granted an enlargement of time up to and
including September 10, 2002, for filing of this Petition.

JURISDICTION

The District Court held jurisdiction pursuant to 28 U.S.C. §
2255; the First Circuit Court of Appeals reviewed the District
Court denial pursuant to 28 U.S.C. §§ 2253 and 1291. This
Court has jurisdiction pursuant to 28 U.S.C. § 1254(1).

STATEMENT OF THE CASE

The complexity of the background to this case cannot be
adequately expressed here. The following description touches
the highest points; a full factual account, provided to the First
Circuit Court of Appeals for bail, is reproduced at
http:/ /hometown.aol.com/ drrodcampbell/.

In 1983, Campbell was the director of synthetic research for
Olin-Hunt Chemical Corporation, supervising ten synthetic
organic chemists and their technicians. He was divesting
himself of his private consulting business to be conflict-free in
order to run the Olin Specialty Chemical plant in Rensselaer,
New York. In the process he had a serious lapse in judgment
that resulted in him delivering a one ounce PCP mixture to a
consulting customer. He was arrested and prosecuted.

At his state trial, the prosecutor portrayed Campbell as the
supplier of a conspiracy, unaware or uncaring of the real
supplier compared to the stature of the arrested suspect. When
it developed that there was virtually no other evidence against
Campbell, despite sixty days of wire intercepts over seven
telephones, the state offered the codefendant a deal for his far
more numerous and serious charges if he would testify that
Campbell was his supplier. He did and Campbell was
sentenced to twenty years.

In prison, Campbell litigated over the dirty tricks that he
alleged in his case and on behalf of fellow prisoners. Six years
later, the Rhode Island Attorney General called Campbell the
most vicious writ-writer his office had ever dealt with.‘

Campbell was paroled after six and one-half years. After
floundering for six months in an effort to restore destroyed
family, Campbell got back into chemistry and let his legal
interests lapse. He became Director of Chemical Research at
Spectra Science Corporation, a Cambridge think-tank company
developing laser and infrared dyes mostly for defensive
military applications.5 On a trip to locate equipment for the
company, Campbell tried to learn what had happened to the

* For example, the State had been required to post a $6,000,000 supersedeas
bond over Campbell’s dirty tricks suit. Campbell v. State of Rhode Island, 89-
CV-0185 (D.R.1.).

5 In his five month tenure, Campbell personally made a dye, vanadyl-
naphthalocyanine, that was written up (unnamed) in the June, 1993, Popular
Science as the camouflage dye against infrared detection of infantrymen.
Monsieur Pasaquay, the research director of Bolle Optical, France, called
Campbell's industrial quantity Lambda 2 dye, for fighier-pilot laser-blinding
protection, “the superb ruby.”

former buyer of his consulting business, Woodman, who had
been the real drug supplier in 1983. Trial trans. V, 60-61.

Re-contact with Woodman soon went past the social with
Woodman wanting to sell Spectra Science infrared-absorbing
dyes to Monsanto Safe-flex Glass in Springfield, Massachusetts,
where his brother-in-law was vice-president. V, 64. This
overture was a ruse, however, for Woodman to persuade
Campbell to make P2P, which he claimed was legal by
producing the 1992 West Criminal Code and Rules for the list
of controlled substances.

Campbell smelled the rat in Woodman and, when simple
“no's” quenched none of the ardor, Campbell researched
Woodman at Rhode Island Federal District Court. An
apoplectic clerk eventually gave Campbell a docket sheet
stamped “SEALED.”

So when Woodman asked for a quid pro quo of a small
sample of P2P for picking up some glassware, Campbell
obliged him with a small sample of chloroacetone teargas. V,
67, 69-70. And when Woodman later switched to wanting a
quaalude raw material, Campbell obliged him with a small
sample of AAOT, a sneezing powder. V, 82. When Campbell
suddenly got fired at Spectra Science with no opportunity to
explain his past, he imagined the hands of enemies in that
termination and resolved to exploit and discredit them.

The game of cat and mouse eventually got out of hand.
Campbell was unable to start the legitimate Grignard Reagent .-
business he wanted before becoming broke. So the ruse
continued with Campbell supplying a non-P2P that simply
smelled like P2P. He designed all the chemical bubbling as
‘show for Woodman’s chemist-trained eye; especially the
solvent choice of (THF, tetrahydrofuran), but then the other
reaction conditions were all meant for the P2P chemistry to fail
and make principally benzylacetate.

Campbell was arrested after nine months of this and
charged with manufacture and distribution and conspiracies to
make both P2P and quaalude. He was persuaded to put on a
wholly apologetic defense, and the D.E.A. chromatogram
analyses appeared to indicate a fraction of a percent P2P

present. So the jury convicted on the P2P counts on instruction
that only a detectable quantity of P2P was necessary for guilt.
The jury acquitted on the methaqualone (quaalude) conspiracy,
but convicted for the “any detectable” instruction. Campbell
was sentenced to 288 months.

After trial, Campbell filed a Rhode Island F.O.I. request
with the Rhode Island Department of Health (R.1.D.O.H.)
Laboratory for its analyses of his samples. D.O.H. had told the
defense that the lab’s analyses had showed P2P; but Campbell
didn’t believe he had messed up and he wanted to understand
how he had. The lab sent the data to Defense Attorney West.

The Health Lab had used exactly the same instrument
setup as the D.E.A. lab in New York. But it had taken more care
in running the samples and had produced better separations of
the chemicals than New York. In the spot where the P2P peak
belonged, there was emptiness; instead, the lab had clearly mis-
identified another chemical, 4-methylacetophenone, as P2P.

Campbell had already submitted the D.E.A. data to Morris
Forensics for evaluation of reliability. Appendix I. Morris
criticized the analyses for their lack of runs of authentic P2P
standards, the lack of duplicate analytical runs per sample to
rule out contamination or mistake, and the low reliability of the
computer matches of mass spectra and infrared spectra actually
obtained when compared with the library spectra. Campbell's
money had run out before the D.O.H. data became available,
however.

So Campbell sought support from industrial chemists. And
he asked his congressional delegation to investigate the fraud
that appeared evident from the two data sets. Union Carbide,
Pfizer, and 3M chemists sympathized, but stayed out of it. The
congressional delegation sent banal letters and hung up on
Campbell.

Campbell sent a sworn criminal complaint to the United
States Inspector General. When he failed to hear anything in
three months he called and was told to file a F.O.I. request. So
he sent a complaint addressed to “Foreman, Currently Sitting
Special Grand Jury For The Southern District Of New York,”
pursuant to 18 U.S.C. §3332. It was returned by the United

States Attorney. He mailed again to Mary Joe White, United
States Attorney, citing In re Grand Jury Application, 617 F.Supp.
199 (S.D.N.Y. 1985). His mailing was returned. Finally, he
mailed to the Honorable John Sprizzo, again pursuant to §
3332, who wrote back saying that he was unable to become
involved.

At the same time Campbell supplied the data to the Court-
appointed expert to his case, Dr. William Suggs of Brown
University. Dr. Suggs had been ill. Nonetheless, he provided an
affidavit that corrected scientific mistakes in his testimony and
the misuse of his testimony at sentencing, and then addressed
D.E.A. Sample 17. First, he agreed with what Campbell had
earlier testified, that the D.E.A. analyses did not show the
solvent components to the mixtures. Solvents were about 90%.
Dr. Suggs reduced his estimate of the highest P2P-containing-
sample possibility from 8% to 0.8%. He alluded to the mixture
no longer being “usable” at 0.8% concentration at all. He also
discussed the fact that the chemistry, which Campbell had
chosen, was more likely than not designed to intentionally fail
to make P2P. But, even more importantly, he examined the
analysis to D.O.H. 1, the first positive testing sample, and
stated that, to his professional judgment, it showed no P2P
down to the detection limits of the analytical method, which
was parts per million. Appendix G.

Campbell filed his § 2255 Application at this stage because
of the A.E.D.P.A. deadline. The Government attempted to
discredit the interpretation of the D.O.H. data, saying it did not
match the D.E.A. samples. Campbell responded by Traverse
and Affidavit, which the District Court refused to file and the
Court returned the Affidavit and exhibits. Appendix F.

Later on, Campbell satisfied the District Court’s concern
that the D.O.H. analyses corresponded to the D.E.A. analyses
by retaining the services of National Medical Services

° To counter continuing Government claims of drug greed as the Defendant's
motive, Campbell swore the fact of getting Woodman’s docket from the R.1.
District Court. Only later did he even realize the legal significance for Court
and US. Attorney personnel being material witnesses to the case. E.g., United
States v. Edwards, 154 F.3d 915 (9% Cir. 1998).

5

Laboratory. Appendix H. Regardless, the Court denied
Reconsideration without further opinion and the Court of
Appeals has adopted the entire decision of the District Court,
twice. Appendices B and C.
. D.E.A. director Asa Hutchinson refers a Campbell letter to
the board of forensic chemists (Appendix M) without ever
obtaining the R.I.D.O.H. evidence. The board recently said
everything is fine.

I. CERTIORARI SHOULD BE GRANTED TO ESTABLISH
DAUBERT v. MERRILL DOW STANDARDS FOR SCIENTIFIC
EVIDENCE IN CRIMINAL ADJUDICATIONS:

Truly scientific controversies are a wholly different creature
capable of higher truth resolution than ordinary cases,
provided the science is understood. In this case, it
convincingly appears that the scientific truth was not judicially
understood and the Courts should have used different
standards to address the meaning of scientific facts both
procedurally and substantively. Due process standards for the
acceptance and evaluation of scientific evidence are plainly
required across the Circuits and certiorari should be granted.

The Petitioner took trial because he was innocent. The
defense was that any P2P “detected” was legally chimeral for
never being more than “trace” and purely accidental if present;
the identifications were done without running known P2P
controls and the analyses were inconsistent between the mass
spectral and infrared spectral laboratories. But the technical
defense was highly disadvantaged by the legal treatment given
scientific issues.

The Defense had made a specific discovery motion for “all
data” in the possession or control of the Government. The
Magistrate enforced the motion at a hearing. Yet, the D.E.A.
only supplied data for the positive-testing P2P samples and the
raw material chemicals that had been seized.” Defense counsel,

* The prosecution knew of the D.O.H. testing because its motion to dismiss
certain counts specifically cited the “screening test” as reason for seeking
dismissal. See Appendix E.

Mr. West, contacted the Rhode Island Department of Health
_ laboratory on his own, but he was verbally told there was P2P
in Campbell's samples. Appendix D. He did not conceive of
the D.O.H. lab making a mistake; and he did not want more
incriminating data.

When the D.E.A. data did come, the copies were largely
unusable. They were skewed and chopped-off in copying;
large portions were unreadable blackness. A great deal of time
was wasted just figuring out what the data was, as late as
cross-examination of the Government chemist, Mr. Fasanello.

The two jurors who might have understood what it meant
for the P2P indications to be “artifacts” of the D.E.A. analytical
method were peremptorily dismissed by the Government.
Eliciting the layman meaning of the data fell to defense
counsel.

“Strictly on these technical issues, I don't
have the capacity to phantom (sic, “fathom”) or
(sic,"all”) the implications of the data that he's
[my client's] attempting to elicit. He thinks he
could do it in a more timely fashion and justice
would be served. I'm really handicapped. I
really don't know what he-[Mr. Fasanello was
being examined] is talking about and [cut off].”
West, IV, 3-4. And any possible backup salvation was
precluded by the exclusion of the defense expert, Dr. Suggs,
from hearing the Government's technical testimony. Campbell
lost trial.

By the time of collateral attack, this advantage of surprise
had been largely overcome. Morris Forensics had seriously
criticized the Government methodology and conclusions for
making marginal identifications from single-run analyses only
showing “trace” amount of P2P. Appendix J. But this type of
evidence was now all but worthless under the changed
standard for relief. Dr. Suggs did an eleventh hour assessment

> Mr. Campbell's notes report that Mr. West quoted D.O.H. chemist Gino
Rabuzzini as saying, “There's rather quite a lot in there.” This statement
conforms to the D.O.H. mistakenly identifying 4-methylacetophenone as P2P.
Vide infra.

of his testimony for oversights and misuses of his statements
just in time for filing of the 2255 Application. Appendix G.
But the piece de resistance was the raw R.I.D.O.H. analysis
data for each and every sample up to Campbell's arrest. When
Campbell saw the data, as a person who had personally run
over 1000 gas chromatogram/mass spectrum (GC/MS)
analyses himself, he immediately knew the Government had a
serious integrity problem with Sample 17. D.E.A. Sample 17
was represented at trial for being Campbell's first positive-
testing sample. Despite the alternate labeling at D.O.H.,
Sample 1? was clearly D.E.A. 17 because that lab was doing
contemporaneous screenings to assist the agents. The visual
difference in appearance is obvious, even to a layman.

Sample “1” D.E.A.

TIC of CH91000!1X17.¢d
A5299; Run at 08:57 AM EST on Wed Maz 17, 1993

6000000
$000000
4000000 DIDENZYLKETONE
0000 PHENYLACETIC
7 AcID
. J :
1000000 cat urine
ingredient
° are
“4 ¥ ss a7 7 ‘ rT T T ¥ + T T ¥ ¥ T T T r ¥ T
4 6 § 10 12
Time (min.)
Sample “1” R.1I.D.O.H.
“3¢ nat ~
was filed by the government before empanelment.®

5 21 U.S.C. § 851(a)(1) provides in pertinent part: No person who stands
convicted of an offense under this part shall be sentenced to increased
punishment by reason of one or more prior convictions, unless before trial, or
before entry of a plea of guilty, the United States attorney files an information
with the court (and serves a copy of such information on the person or
counsel for the person) stating in writing the previous convictions to be relied
upon. xk

6 A jury was empanelled on January 27, 1994. As used in 851(a)(1), "before
trial" means prior to jury selection. See United States v. Cartagena-
Carrasquillo, 70 F.3d 706, 715 (ist Cir. 1995) (citing Kelly v. United States, 29
F.3d 1107, 1110 (7th Cir. 1994)).

D. The Constitutionality of 21 U.S.C. § 851

- Campbell contends that 21 U.S.C. § 8517 is unconstitutional on
its face because it provides for increased penalties based upon
prior state court felony drug convictions, thereby violating the
prohibitions against ex post facto laws, bills of attainder and
double jeopardy, and because it violates the Ninth and Tenth
Amendments. Campbell also asserts that the court's application
of this provision violated his right to due process and was in
excess of the court's jurisdiction under Article III.

Since Campbell has not demonstrated "cause" for failing to
raise these claims on appeal, he is procedurally precluded from
litigating them now.

Moreover, even if Campbell could raise these issues, his

arguments rest on the erroneous premise that the consideration ©

of his prior convictions constituted either a redetermination of
his guilt or an additional punishment for the state law
violations. The Supreme Court has "repeatedly upheld
recidivism statutes ‘against contentions that they violate
constitutional strictures dealing with double jeopardy, ex post
facto laws, cruel and unusual punishment, due process, equal
protection and privileges and immunities." Parke v. Raley, 506
U.S. 20, 27 (1992) (quoting Spencer v. Texas, 385 U.S. 554, 560
(1967) (internal quotations omitted)). It has also held
that"[e]nhancement statutes * * * do not change the penalty
imposed for the earlier conviction." Nichols v. United States, 511
U.S. 738, 747 (1994). Sentencing enhancement provisions are
not bills of attainder. See Nixon v. Administrator of General
Services, 433 U.S. 425, 468 (1977) (key features of a bill of
attainder include a legislative determination of guilt and
imposition of punishment upon an identifiable individual with
(sic) provision of the protections a judicial trial).

7 21 U.S.C. § 851 simply sets forth the procedures to be employed in applying
the increased penalties delineated elsewhere in Title (sic) 21. To the extent
that Campbell seeks to challenge the substantive provision, the appropriate
reference is to 21 U.S.C. § 841(b)(1)(C).

Pa tr oe me Se. Te ee eee

a ee ey aS eee

E. Knowledge and Intent

Campbell argues that, because P2P is only a precursor to—
methamphetamine, the government was required to prove that
he knew that the P2P could be used to manufacture
methamphetamine. This argument, too, is procedurally barred.

Even if Campbell could raise the issue, Campbell is incorrect
in asserting that the government was required to prove that he
knew that P2P could be used to manufacture
methamphetamine. Section 841(a)(1) makes it unlawful to
"knowingly or intentionally * * * manufacture * * * a controlled
substance." 21 U.S.C. § 802(6) defines "controlled substance" as
"a drug or other substance, or immediate precursor, included in
schedule I, II, Ill, IV, or V of part B of this subchapter." Since
P2P has been designated as a schedule II "immediate
precursor", (sic) 21 C.F.R. § 1308.12(g)(1)(i), it is a "controlled
substance" within the meaning of § 841 and the government
was required to prove only that Campbell knowingly or
intentionally manufactured P2P. :

In any event, the evidence is overwhelming that, in fact,
Campbell did know that P2P was a precursor to
methamphetamine. The evidence also undercuts Campbell's
argument that his guideline sentencing range was calculated
on the erroneous premise that he possessed P2P "for the
purpose of manufacturing
methamphetamine", (sic) thereby triggering a conversion
equivalent of 416 grams of marijuana per gram of P2P rather
than 75 grams of marijuana per gram of P2P. See Drug
Equivalency Tables, U.S.S.G. § 2D1.1 comment. (sic) (n.10).

More importantly, Campbell's challenge to use of the 416
multiplier was considered and rejected by the First Circuit on
direct appeal. United States . Campbell, 61 F.3d at 985-86.
Although Campbell now attempts to recharacterize and to
provide additional legal theories in support of his argument,
the gravamen of his claim remains the same as the one rejected

on appeal and will not be revisited. E.g., Singleton v. United
States, 370 F.2d 862, 864 (1st Cir. 1967). .

F. The Sentencing Enhancement

Campbell argues that the offense level enhancements for
obstruction of justice and abuse of his special skill as a chemist,
and the upward departure based on his past criminal conduct
and the likelihood that he would commit other crimes in the
future were erroneous. Once again, this is simply a rehash of
arguments made and rejected on direct appeal. Consequently
they cannot be raised in Campbell's § 2255 motion.

Campbell attempts to circumvent that prohibition by
asserting that the matter should be reevaluated in view of "new
evidence." However, the "new evidence" consists of nothing

more tharrthe previously rejected claims of evidence tampering
- and perjury. Thus, Campbell's arguments lack any factual
foundation.

G. Imposition of the Costs of Supervision

Finally, Campbell argues that this Court had no authority to
impose the costs of supervised release because Campbell was
indigent. Since Campbell had failed to present any "cause" for
not raising this issue on appeal, he is procedurally barred from
raising it now.

In addition, Campbell ignores the fact that the Court
deferred payment of the costs of supervision until Campbell
was released from prison and could begin using his
considerable talents to earn the money to pay those costs.

Conclusion

For the above reasons, Campbell's § 2255 motion is denied.
Because Campbell is not entitled to relief on any of his claims,
his motion for partial summary judgment is also denied.

IT IS SO ORDERED.

[s/
Ernest C. Torres
Chief Judge

May 16, 2000

Ts

UNITED STATES COURT OF APPEALS
For The First Circuit

No. 00-2399
RODERICK A. CAMPBELL,
Petitioner, Appellant,
v.
UNITED STATES,

Respondent, Appellee.

Before

Boudin, Chief Judge,
Selya and Lipez, Circuit Judges

JUDGMENT

Entered: September 6, 2001

Roderick Campbell ("Campbell") has appealed from the
denial of his motion for post-conviction relief pursuant to 28
U.S.C. § 2255,and we treat his notice of appeal as a request fora
certificate to file a memorandum in support of a request for a
certificate of appealability, though, and the time for doing so
has passed. "If no sufficient memorandum has been filed by the

ee eee

time set by the clerk, the certificate may be denied without
further consideration. The effect of a denial is to terminate the
appeal.” 1st Cir. Loc. R. 22.1(b). We have reviewed Campbell's
submissions below, and we see no reason to make an exception
here and allow Campbell to proceed, despite his failure to
comply with Local Rule 22.1(b). |

Many of his arguments restate those already rejected by this
court in Campbell's direct appeal, and his new arguments lack |
merit. His new arguments regarding allegedly exculpatory
evidence would not succeed, because he has failed to show :
cause for failing to raise them earlier; the arguments do not
establish his actual innocence of the charges as a whole; he has
failed to show the evidence was unavailable to him, see United
States v. Rodriguez, 162 F.3d 135, 147 (1st Cir. 1998), and even if
the government should have turned over the results in
question, any error is harmless.

His ineffective assistance of counsel arguments fail as well.
Campbell is not entitled to a perfect defense, only to a
reasonably effective one, Singleton v. United States, 26 F.3d 233,
238 (1st Cir. 1994); and especially since Campbell himself was
readily available and qualified to assist counsel with the more
technical aspects of the evidence, we see no reason to allow
Campbell to pursue this charge further. Moreover, the court's
file clearly reflects that the required information pursuant to 21
U.S.C. § 851(a) was filed several days before the jury was
empanelled, so no timeliness argument could have been
pursued by counsel.

Finally, no Apprendi problem is presented here, because
Campbell's ultimate sentence -- 24 years -- was within the
default maximum sentence applicable to the offense. See 21
U.S.C. § 841(b)(1)(C) (maximum sentence for Schedule II
controlled substance is 30 years, where defendant has prior
conviction for drug felony); see also Apprendi v. New Jersey, 120
S.Ct. 2348 (2000), 120 S.Ct. at 2362 (fact of prior conviction need
not be determined by jury beyond reasonable doubt); United

States v. Baltas, 236 F.3d 27, 41 (1st Cir.) (no Apprendi error
when sentence is within default statutory maximum,
regardless that drug quantity not determined beyond a
reasonable doubt); cert. denied, 121 S.Ct. 1982 (2001).

The request for a certificate of appealability is denied and
the appeal is terminated. The motion to proceed in forma
pauperis is denied as moot.

By the Court:

Acting Clerk.

cc: Roderick A. Campbell
Kenneth P. Madden, Esq.

Certified copies to: Honorable Ernest C. Torres and Mr. David -
DiMarzio, U.S.D.C. Clerk.

UNITED STATES COURT OF APPEALS
For The First Circuit

No. 00-2399
RODERICK A. CAMPBELL,
Petitioner, Appellant,

Vv.

UNITED STATES,

Respondent, Appellee.

Before

Boudin, Chief Judge,
Selya and Lipez, Circuit Judges

ORDER OF COURT
Entered: November 26, 2001

The court is in receipt of petitioner Roderick Campbell's
("Campbell's") "Motion To Withdraw Decision" and "Petition
for Certificate of Appealability" and supporting memorandum.

The court previously had ordered Campbell to file a
memorandum in support of a request for a certificate of
appealability by May 2, 2001; see order dated 4/11/2001. We
presume Campbell received this order, order dated 4/11/2001.
We presume Campbell received this order, since Campbell
already had advised the court of his correct mailing address at
the time the order issued, and since he apparently was aware
of other language in that order which reinstated the appeal.

Nevertheless, we have reviewed and considered fully the
substantive arguments presented in Campbell's recent
submissions. We treat the instant motion as one for rehearing
and the memorandum as one in support of the motion for
rehearing. For the reasons given in our judgment dated
September 6, 2001, we deny the petition for rehearing.

By the Court:

Janice O'Neil, Acting Clerk

By: __Julie Gregg
Appeals Attorney

cc: Roderick A. Campbell
Kenneth P. Madden, Esq.

UNITED STATES DISTRICT COURT
FOR THE DISTRICT OF RHODE ISLAND
RODERICK A. CAMPBELL
v. | 93-CR-0049-T -

97-CV-0274-T
UNITED STATES OF AMERICA

AFFIDAVIT

I, Albert B. West, Esq., being duly sworn, hereby make affidavit
and state that:

1. That in preparation for trial in the captioned proceedings,
I spoke with representatives of the Rhode Island Department of
Health Laboratory.

2. That I was advised by Mr. Gino Rebussini that, in fact,
detectable amounts of P2P were found in the samples that were
analyzed by that office.

3. That as a consequence of receiving this information, I
cautioned and recommended that witnesses from the State Lab
not be called, since in my view their testimony would be
supportive of the government's position and contrary to
positions being advanced by the Defendant.

Ls/
Albert B. West, Esq.

Subscribed and sworn to before me at Cumberland, Rhode
Island, this.10th day of July, 2000.

D

/s/ Amy J. Manning _
Notary Public
Comm. Expires: __10-30-01

IN THE UNITED STATES DISTRICT COURT

FOR THE DISTRICT OF RHODE ISLAND

UNITED STATES OF AMERICA

Vs. Cr. No. 93-049T

RODERICK CAMPBELL
HAROLD FARRELL

ee ere NN

GOVERNMENT'S MEMORAN DUM IN SUPPORT
OF ITS MOTION TO DISMISS COUNTS

The Government has moved to dismiss Courts XI, XII, XIII,
XIV, XV, XVI, XVII of the instant indictment.

Counts XI, XII and XIII charge defendant Harold Farrell
with distribution of the controlled substance phenylacetone.
Subsequent analyses by a chemist of the Drug Enforcement
Administration regarding those substances reflected in Counts
XI, XII and XIII are negative for the presence of any controlled
substance.

Count XVII charges defendants Roderick Campbell and
Harold Farrell with possession with intent to distribute
phenylacetone. The subsequent analysis by a chemist of the
Drug Enforcement Administration regarding the substance
reflected in Count XVII is negative for the presence of any
controlled substance.

Count XIV charges defendant Roderick Campbell with the
attempted distribution of phenylacetone. Counts XV and XVI
charge Defendant Harold Farrell with attempted distribution of
phenylacetone. The substance reflected in each of those counts
were known to the government not to contain controlled
substances based upon the results from preliminary field tests.
However, the substances were represented by the defendants
to be phenylacetone. In light of the negative analyses for

Counts XI, XIl, XIII, and VIL the government does not
presently believe that it can sustain its burden of proof with
regard to the attempt crimes charged in Counts XIV, XV and
XVI.

Wherefore, the government moves this Court to dismiss
Counts XI, XII, XIII, XIV, XV, XVI, and XVII of the indictment.
Respectfully submitted,
UNITED STATES OF AMERICA

By its attorneys,

Edwin J. Gayle
United States Attorney

[s/

KENNETH P. MADDEN
Assistant U.S. Attorney

UNITED STATES DISTRICT COURT
District of Rhode Island

January 25, 1999

Roderick Campbell

F.C.I. Schuylkill

03869-0706

P.O. Box 759

Minersville, Pa 17954-0759

Dear Mr. Campbell,

I am returning the enclosed affidavit which you apparently
forward (sic) to us with your objection to the Government
motion to consolidate.

I am returning the document to you for your necessary
action.

Sincerely,

James E. Webb
Deputy Clerk

One Exchange Terrace, 119 Federal Building & Courthouse,
Providence, R.I.

F

IN THE UNITED STATE DISTRICT COURT
FOR THE DISTRICT OF RHODE ISLAND

UNITED STATES OF AMERICA
v. ; 93-CR-0049

RODERICK A. CAMPBELL

AFFIDAVIT

I, John William Suggs, do depose and swear the following
under oath:

1. Iam the John William Suggs who has been an expert
witness for the defense in the above captioned case and I have
personal knowledge of the facts presented herein.

2. My time to interview with Mr. Campbell was necessarily
limited due to my professional responsibilities at Brown
University and the security arrangements at the Intake Service
Center. | met with Mr. Campbell two times for a total of no
more than 90 minutes. The rest of the preparation was with
counsel, Attorney Albert West. While Mr. Campbell was very
knowledgeable about organic chemistry, Mr. West was not,
although he tried hard to understand what Mr. Campbell and
myself had to say about organic chemistry.

3. Mr. Campbell has explained to me the use made of my
estimate that the samples contained a maximum of eight
percent P2P and a confusion amounting to a mistake made for
the unqualified use of that statement.

4. By the eight percent figure, which I tried to indicate-was an
approximation, I was referring to the components in the

G

chromatograms. These are compounds of a similar volatility. ,
In organic chemistry, we would refer to them as the higher
boilers, or compounds with higher boiling points. As Mr.
Campbell pointed out to me, in all the chromatograms, the first
two minutes of the sample run is not analyzed, because that
region contains the low boiling solvent portion of the sample.
This is on the order of 90 percent of the sample; so the amount
of P2P in the total sample (if the P2P identification is valid) is
on the order of less than 1 percent of the total, low boilers and
high boilers together.

5. The estimate of 90 percent low boiling material comes from
sample 18. The percentage is a weight percent.

6. Mr. Campbell argues that the peak identified in the
chromatograms as P2P is sometimes the compound 4-
methylacetophenone-and sometimes the closely related
compound 2-methylacetophenone. To clarify the argument, a
drawing of the structures of the compounds in question is
shown below:

A
or Oe Lo
CH; H3C

P2P 2-methylacetophenone 4=methylacetophenone
boiling point 216 _ boiling point 218 boiling point 226

These are what is called isomers, compounds with the same
number and types of atoms, but connected in different ways.
The analysis columns used to separate the mixture into
different components did its job on the basis of boiling point of
each component. The boiling points of these three isomers are
very similar, and one would expect them to appear close to one
another on a GC-MS or GC-FTIR analysis.

7. The synthesis, as described in detail to me by Mr. Campbell,
involved addition of chlorine to toluene in water to make the

a a ae

compound benzyl chloride. This was then reacted after some
purification with magnesium metal to make the compound
benzyl magnesium chloride. The presence of 2-
methylacetophenone and 4-methylacetophenone are consistent
with Mr. Campbell's description, since these compounds
would arise from the reaction of chlorine with toluene, giving
several chemical compounds at the same time. To clarify with
diagrams:

H3 HCl H3 H2 CHs
+ Cl, —s + > +
a Cc
Cl

Above is shown the reaction of chlorine with toluene. Four
products are expected. Traces of iron will favor formation of
the last three. As we shall explain, only the first of these
products goes on to P2P. The last product shown is formed in
the smallest amounts. Once the chlorine reaction is over,
reaction with magnesium (Mg) will give four main products:

H3 H3
i a. [on
) ¢ CIMg
; CH; Hg
P! ex Mg — CL ‘
2) cl MgCl
eG -CH2CH2
OM «OG
Ci H»MgCl
4) Ey" + Mg ——» ie

Only reaction 4 will go on to give P2P. Reactions 1 and 2 will
give 4-methylacetophenone and 2-methylacetophenone,

respectively. Reaction 3 gives bibenzyl, which does not react
further. This bibenzyl compound is identified as a major
component of the analyzed mixtures. Also consistent with Mr.
Campbell's description of his synthetic route is the presence of
benzyl alcohol and benzyl acetate in the mixture. They arise
from benzyl chloride as summarized below:

a H2OH ococ
ES. + — ee = acetate ia "

8. It is a well-established fact that attempts to form benzyl
magnesium chloride (by reaction 4) are inefficient and usually
the reaction shown in reaction 3 is the major and often the only
pathway. Thus, one would expect a very low, and possible
zero, yield of P2P by the route Mr. Campbell used. His route
needed reaction 4 to work in order to get any P2P. There is
scientific basis, from the array of products in the analyzed
samples, for Mr. Campbell's contention that he chose a route to
P2P he expected to fail and produce no P2P because of the
problems with reaction 4.

9. While I have not had a chance to personally study the
R.I.D.O.H. chromatograms, due to my schedule, I have seen the
reduced, photocopied version of one chromatogram, of sample
17. | agree with Mr. Campbell's analysis that the resolution is
better than the DEA chromatograms. Further, I agree that, if
P2P is poorly resolved from the methylacetophenone isomers
in the DEA analyzed samples, it should be better resolved in
the R.I.D.0.H. chromatograms, leading to two separate peaks
or at lest (sic) peak broadening. If the data on the rest of the
R.1.D.O.H. chromatograms are the same as on the one sample |
have seen, I would be convinced that there was no P2P in these
samples, down to the limits of detection of the analytical
method. Instead, i would conclude that the peak identified as
P2P is most likely a methylacetophenone isomer.

10. Had I been appraised and examined on the above topics
during my testimony, I would have testified then exactly as I
have presented these facts now.

Further your Deponent Sayeth Not,

Ls/
John William Suggs
July 15, 1997

STATE OF RHODE ISLAND
COUNTY OF PROVIDENCE

Subscribed and sworn to before me at Providence, RI, this 15th
day of July, 1997.

—

Ls/
Notary Public

Comm. Expires: 6/24/01

NATIONAL MEDICAL SERVICES, INC.
Toxicology Specialists Worldwide Since 1970

March 5, 2001

Albert West, Esq.
Manning & West
3460 Mendon Road
Cumberland, RI 02864

Re: Roderick A. Campbell
Your File # L10113
NMS Expert Services No. N00194

Dear Mr. West:

You and your firm have retained National Medical Services,
Inc., represented by Lee Blum, Ph.D., as consultants in
Toxicology in the above captioned case. You have been
furnished a description of National Medical Services, Inc., as
well as a copy of my Curriculum vitae. You have requested
that I review pertinent documents and records and form
conclusions and opinions regarding the analysis of D.E.A. item
17 indicated to have been obtained from Roderick A. Campbell.

In order to comply with this request, you have supplied me
with the following relevant documents and records:

1. A copy of a sworn declaration of Roderick A. Campbell.

2. Acopy of an affidavit of John Suggs dated July 15, 1997.

3. Copies of analytical data from the ~ Rhode Island
Department of Health.

4. Copies of analytical data from the U.S. Department of
Justice, Drug Enforcement Administration.

H

-

5. A copy of a letter to David Uliss, Ph.D., from Roderick
Campbell dated May 24, 2000.

6. A copy of a letter to Kenneth P. Madden, Esq., from
Roderick Campbell dated June 22, 2000.

7. A copy of an affidavit from Roderick Campbell dated
November 8, 1998.

8. A copy of a document entitled: The government violated
the Defendant's due process right by not disclosing to the
defense the exculpatory Rhode Island Department of
Health analysis.

9. A copy of a page of what appears to be transcripts from
testimony with attachments.

10. A copy with an affidavit from John W. Suggs dated July 11,
1997.

11. A copy of an affidavit from Wayne A. Morris dated June 12,
1997.

12. A copy of a letter to Albert West from J. William Suggs re:
R. Campbell dated February 2, 1994.

In addition to the above documents and records, I have been
asked to assume the following:

1. D.E.A. Samples 17, 18, 19, 20, 22, 23A, and 24 correspond to
D.O.H. Samples 1, 2, 3, 4, 6, 7A, and 8 respectively;

2. Both the D.E.A. and D.O.H. laboratories performed their
respective analyses on Hewlett-Packard 5800 gas
chromatographs with factory manufactured HP-1 columns;
and

3. The only pre-analytical treatment of the samples was
dilution with methanol and possible filtration of any
precipitated solids.

It should be noted that I have made these assumptions with no
substantial documents or records. I did not receive any
specimen chains of custody, sample preparation procedures,
analytical procedures, concurrent instrument conditions and
parameters, or analytical data from standard or quality control
samples, among others.

Based on the submitted documents and records, the
assumptions given, as well as my knowledge, education or
experience, it is my opinion, with a reasonable degree of
scientific certainty that the total ion chromatograph (TIC) from
the gas chromatograph/mass spectrometry (GC/MS)
analytical data identified as D.E.A. item 17 appears different
from the total ion chromatograph (TIC) of the GC/MS data
identified as D.O.H. item 1?.

The following support the above opinion and conclusions:

1. The three peaks identified from the data submitted for
D.E.A. item 17 indicate 1-phenyl-2-propanone (P2P) at
retention time 4.99 minutes; and 1,3-dipheny]-2-propanone
at retention time 8.19 minutes.

2. The TIC obtained from the analysis of D.O.H. item 1?
recognized at least 9 chromatographic peaks with more
recorded in the chromatogram, but not indicated in the
data report. :

3. If all things are equal between the D.E.A. and the D.O.H.
laboratories including the amount analyzed, the
preparation of the sample, the analytical column 30%
(identified as 1,3-diphenyl-2-propanone at 8.19 minutes),
respectively, of the total. The peak identified as P2P in
D.O.H. sample 1? at retention time 6.50 minutes comprises
13.3% of the total. In addition, the peak identified as P2P in
the D.E.A. item 17 at retention time 3.74 minutes is the
base (or highest) peak, whereas in the D.O.H. analysis, the
P2P peak at 6.50 minutes is 50% of the base peak which
occurs at 10.81 minutes. Likewise, using the peak identified
as P2P at 3.74 minutes on D.E.A. item 17 at retention time
3.74 minutes as the base peak, the peaks at 4.99 and 8.19
minutes have peak heights of 35% and 58.3%, respectively.
A comparison of peak heights on the D.O.H. item 1? GC
TIC does not identify peaks whose heights are

approximately 89,000 counts (35% of 255702, the peak
height corresponding to the chromatographic peak at
retention 6.50 minutes) or approximately 149,000 (58.3% of
255702) at retention times later than the 6.50 minutes peak.

In addition to D.O.H. 1?, the D.E.A. item 17 chromatogram,
which contained three chromatographic peaks, did not
appear to match the chromatographic profiles of D.O.H.
samples 2, 3, 4, 6, 7A, 7B, or 8. Sample 2 demonstrated at
least six chromatographic peaks; sample 3 exhibited at least
four peaks; sample 7B showed at least 7 peaks; and sample
8 recognized five chromatographic peaks. Furthermore the
relative size of the peaks in D.E.A. item 17, did not
correspond to the listed D.O.H. samples when compared
one to the other within each sample.

With the assumption of the identical sample preparation,
the amount analyzed, and the gas chromatographic
conditions (including the analytical columns, temperature
programs, etc.), the chromatographic profiles of D.E.A. item
17 from the GC/MS and the GC/FTIR analyses should be-
similar. Examination of the GC/MS chromatographic
profile exhibits three chromatographic peaks at 3.74, 4.99,
and 8.19 minutes. The GC/FTIR chromatogram shows
numerous small peaks from approximately .5 through
approximately 1.5 minutes, a large single peak at
approximately 3 minutes, and at least one (if not more)
small peak(s) just prior to 5.00 minutes.

If additional information or documents become available that
may affect the above opinion and conclusions, please forward
them to me for further evaluation.

Respectfully,

Lee M. Blum, PhD., DABFT
Forensic Toxicologist

In the County of Mercer, Sc.

AFFIDAVIT

I, Martin Bramson, do’ swear under oath the following
statements and conclusions as true and accurate to be best of
my knowledge and belief:

1. lama degreed chemist and pharmacist with the attached
educational background. I have studied all of the data in the
case United States v. Campbell, 93-CR-0049, and in the habeas
corpus application, 97-CV-0274. This includes all data
generated by both the Drug Enforcement Administration
Northeast Regional Laboratory (D.E.A.) and the Rhode Island
Department of Health (D.O.H.). I have also evaluated the
reports of Dr. William Suggs, of Morris Forensics, and of
National Medical Services Laboratory. I have also reviewed
the trial record for factual background.

2. Based on my review of all the information available and
using my technical background and experience, I have been
asked to take this data and these reports to their ultimate
conclusions, where I conclude that other reviewers have not
been complete.

3. It is-my first conclusion to a scientific certainty that the
R.I.D.O.H. has misidentified the chemical 4-methylacetopheone
(abbreviated 4-MA) as the chemical phenyl-2-propanone (P2P)
in each and all of the analyses appearing to show the presence
of "P2P." They are in fact showing the presence of "4-~MA."

4. It is my second conclusion to a scientific certainty that the
standard screening, as I know these screening tests to be done,
performed by the R.I.D.O.H. would have located P2P in these
samples down to concentrations of parts per million. I conclude
from study of the data, including the absence of a visual peak
or shoulder in D.O.H. chromatograms in the region of expected
P2P appearance, that there is no P2P in these samples down to
parts per million concentration.

5. It is my third conclusion to a scientific certainty that the
D.E.A. mass spec/chromatogram of Sample 17 is anomalous to
all the other data available on that sample. I state that the most
likely explanation for this anomaly is that the mass spectral
sample has been falsified. I state this conclusion based on the
lack of reporting of the major chemicals to the Sample 17
mixture by the D.E.A.'s own infrared lab being irreconcilable
scientifically. I further state this conclusion based on the fact
that Dr. Blum's exhaustive cross-referencing forces a reviewer
to conclude that D.E.A. 17 is D.O.H. 1?. I state this finally
based on the factual background in the trial testimony and the
transcripts of surveillance-taped conversations that Mr.
Campbell disclaimed ever running a "traditional" synthesis and
his statement is supported by all the data except the D.E.A.
mass spectrum/chromatogram.

6. It is my conclusion based on my study and the
appearance of the mixture chromatograms that D.E.A. Sample
17 corresponds to D.O.H. Sample "1?" to a scientific certainty.
7. Finally it is my conclusion to a scientific certainty that these
mixtures are an order of magnitude more dilute in high boiling
components (e.g., 4-MA) than was represented at the trial of
this case. I agree with Dr. Suggs' appreciation that the D.E.A.
chromatograms failed to show the solvents. It is my conclusion
that no amphetamine products could be made from these
mixtures, even if they legitimately contained the P2P shown in
the D.E.A. chromatograms, due to their extreme dilution and
low purity.

Subscribed under penalty of perjury,
LS/

Martin Bramson

AFFIDAVIT

STATE OF FLORIDA
COUNTY OF ORANGE

BEFORE ME, the undersigned authority, personally
appeared WAYNE A MORRIS, who after being sworn deposes
and says as follows:

1. That he is over 21 years of age and that the facts, opinions,
or conclusions set forth in this Affidavit are of his own personal
knowledge.

2. That he is a chemist holding a Master's Degree in Physical
Chemistry (thesis area in infrared spectroscopy), and he is in
private practice as co-owner/president of Morris-Kopec
Forensics, Inc., P.O. Box 1065, Goldenrod, Florida 32733-1065,
telephone number 407-678-5508.

3. That he has been in private practice since March, 1986, and
previously was employed as a crime laboratory analyst by the
Florida Department of Law Enforcement (FDLE) from March,
1976 to March 1986.

4. That he has been qualified as an expert in the area of drug
analysis in State Courts of Florida, and Federal Courts-in Texas
and Florida.

5. That he has attached hereto a true and correct copy of his
experience and qualifications.

6. That the Drug Enforcement Administration has registered
Morris-Kopec Forensics, Inc. as an analytical laboratory
covering all schedules of controlled substances.

7. That he has developed and manufactured field test kits for
controlled substances, including Cocaine, and as part of his
routine business, and that he is co-author of a patent for a field
test kit for Methaqualone and Mecloqualone.

8. That he has testified as an expert in Courts of Florida and
Federal Court as to the results of his analyses in over one
thousand cases.

9. That he has routinely used infrared spectroscopy, gas
chromatography and gas chromatography-mass spectroscopy
for the identification of controlled substances.

10. That he has been qualified as an expert in Courts of Florida
and Federal Courts in the use of gas chromatography and gas-
chromatography-mass spectroscopy for the identification of
controlled substances.

11. That in mass spectroscopy, the quality of the comparison of
the mass spectrum of the unknown to that of a known
(standard) is of utmost importance. The generally accepted
standard for library matches with an unknown compound
have numerical values above 98%. In this matter, the library
search for the results of the mass spectral analyses gave
numerical values of 94 and below. These levels of matching are
far below the generally accepted standard and indicate a low ~
level of reliability for the identifications made in this case.

12. That in mass spectroscopy, the initially acquired spectral
data may be altered by the addition and/or subtraction of
other spectral data arising from background spectra or co-
eluting compounds. Such manipulation of data must be done
carefully in order to prevent the loss of spectral information
arising from the unknown compound or the addition of
spectral information arising from other compounds. The loss
or addition of such data can result in-erroneous identification.
In this matter, the initial mass spectral data have been altered
by addition, subtraction, and normalization techniques

resulting in identifications of the unknown compounds as P2P
with low levels of confidence.

13. That in this case, the mass spectra do not reliably identify
the unknown compounds as P2P since the small amounts of
P2P alleged to have been identified by the library searches are
obtained by the substraction (sic) and addition of spectral data
arising from overlapping compounds having very similar mass
spectra. The absence of the fragment at m/e 119 in the P2P
spectrum differentiates P2P from these other compounds but
the absence of the m/e 119 peak could have been caused by the
manipulation of the spectral data.

14. That in gas chromatography, the repeatability (precision) of
the retention times for peaks representing the same
compound in different samples analyzed under the same
chromatographic conditions is mandatory. In this matter, the ~
agreement of retention times is not as high as should be
expected. Similar chromatographic conditions are reported on
the data but the retention times for the peaks alleged to be P2P
do not show good precision.

15. That, in the case of compounds having closely similar or
identical retention times under the same _ set of
chromatographic conditions, the agreement of retention times
arising from an unknown compound with a retention time for
a known standard, only indicates the possible presence of one,
any, or all of the co-eluting compounds. In this matter, the
chromatographic data only indicates-the possible presence of
P2P and/or other compounds arising from the chemical
syntheses used in the production of these samples.

16. That, the spectra identified as P2P in this case are missing a
prominent shoulder about 1900 cm! and several weak bands at
approximately 1300 cm and between 2850 and 2650 cm"
which are clearly present in the P2P infrared spectra used as a
standard. Although data obtained from gas chromatography-
Fourier Transform Infrared Spectroscopy (GC-FTIR) are

expected to show slight differences from conventional infrared
spectra, the observed differences in this case are significant.

17. That, according to the testimony of the Government's
expert, the P2P standard was at least 98 percent pure. Infrared
analyses of samples having 98 percent purity or better result in
infrared spectra of essentially the pure compound.

18. That, the band in an infrared spectrum are produced by
structural characteristics of the molecule. Very strong, strong,
medium, weak and very weak bands in an infrared spectrum
are explained by the selection rules of infrared spectroscopy
which are based upon the structure and symmetry of the
molecule and NOT upon the concentration of the compound in
the sample analyzed. If strong bands and weak bands are
present in the standard spectrum of a compound, they would
also be present in a spectrum obtained from an unknown
sample of the same compound, regardless of concentration.

19. That, the weak bands observed in the standard spectrum
are not present in the spectra obtained from the samples in this
case. For the identification of an infrared spectrum to be made
by comparison with a standard spectrum, _ it is important that
all the bands in the unknown spectrum have a relative height
relationships (sic) which is similar to the relative height
relationships in the standard spectrum. This is not occurring in
this case.

20. That, mixtures of compounds co-eluting from the gas
chromatograph's column will produce a spectrum which is an
additive result of the individual spectra of each component. ,

21. If an infrared spectrum is produced by co-eluting
compounds, the observed spectrum may be misidentified as a
compound not contained in the sample. Weak bands and
shoulders may not be seen due to peak broadening and
changes in peak height which, upon normalization, may reduce
a band below the noise level of the baseline. Medium and

strong bands may arise from only one of the co-eluting
compounds.

22. That, considering the poor quality of the library matches
between the known and unknown mass spectral data, the
missing peaks and shoulders in the infrared spectra, and the
poor agreement of the gas chromatographic retention times
available in this matter, there is a serious question as to the
scientific reliability of the identifications of P2P in any of the
samples analyzed, including those reported by the Drug
Enforcement Administration's Laboratory and by the Rhode
Island Department of Health Laboratory.

FURTHER AFFIANT SAYETH NOT.

/s/
WAYNE A MORRIS

I HEREBY CERTIFY that on this day, before me, an officer
authorized to administer oaths and take acknowledgments,
personally appeared Wayne A. Morris, known to me to be the
person described in and who executed the foregoing
instrument, who acknowledged before me that he executed
same, that I relied upon the following from (sic) of the above
named person:

and that an oath (was) taken.

Witness my hand and official seal in the County and State
last aforesaid this 24th day of June, 1997.

/s/
Notary Public

JACQUELINE F. BEAMS
Printed Name Of Notary

My Comm. Expires: 2/29 /2000
Comm. # CC 527031 (Seal)
Bonded Through
Atlantic Bonding Co., Inc.

JUNE 26, 1993
DEA SUSPENDS HEAD OF ITS OFFICE IN PROVIDENCE

The move by the federal Drug Enforcement Administration
comes after Mayor Cianci received a phony letter saying he
was the target of an investigation.

By DAN BARRY
and LAURA MEADE KIRK
Journal-Bulletin Staff Writers

PROVIDENCE - The federal Drug Enforcement
Administration's local agent in charge has been placed on paid
leave, after an investigation into a phony letter warning Mayor
Vincent A. Cianci, Jr. that he was the target of a drug
investigation. :

Vincent F. Furtado, a longtime DEA agent who has headed
the Providence office for the last two years, was relieved of his
duties - and his gun - last week, an agency spokesman said
yesterday.

The spokesman confirmed that there is "an issue of a letter."
But he said that Furtado's departure was primarily based on
questions regarding the local DEA office's relationship with
state and local departments.

Sources, however, Say the decision to remove Furtado was
prompted by a bogus letter that Cianci received in March - and
which has been traced to Furtado's office.

The one-paragraph letter, purporting to be from a
Providence police officer, warned Cianci that he was the target
of a drug investigation.

The writer said that the head of the drug unit, Inspector
Urbano Prignano, and Henry Roy, #4 officer on loan to the
DEA, "have been overheard talking about your (Cianci's) use of
drugs," and that "there is talk of a meeting with the US.
attorney about this and the ability of the PD (police
department) to catch you."

The letter also said that "there seems to be an informant that
has the information needed to set you up" - presumably for the
purpose of arresting Cianci.

Providence Police Chief Bernard Gannon emphasized
yesterday that his department has not received any accusations
of Cianci being involved with drugs. "To my knowledge, we
have never had any investigations into the mayor concerning
any criminal activities whatsoever," Gannon said.

Cianci confirmed yesterday that he had received the
unsigned letter. "It said something about beware of two
policemen who would try to set you up, and it mentioned two
police officers," Cianci said.

The mayor noted that the letter turned out to be "totally
false" and he described Prignano and Roy as "two of the finest
police officers that we have."

There is no conclusive evidence liking Furtado to the letter.
However, sources say that Furtado has been squabbling with
Providence police over the handling of drug investigations,
and the letter was interpreted by city officials as an attempt to
discredit Prignano and Roy.

Cianci forgot about the letter - until three weeks ago, when
he was visited by two agents from the DEA's professional
services unit in Washington. He said they told him they had
reason to believe the letter originated at the DEA's Providence
office.

Sources say that DEA investigators found the text of the
letter in the carbon cartridge of a typewriter in the DEA's local
headquarters. But the office is used by several DEA agents and
other law-enforcement officers.

DEA spokesman Jack Kelly declined to discuss the letter.
Instead, he emphasized that the action against Furtado was
prompted by concerns about the operation of the Providence
office.

"The primary issue is administrative in nature," Kelly said.
"It's the DEA's relationship with state and local authorities that
is being reviewed."

Prignano declined comment, as did acting U.S. Attorney
Edwin Gale. Furtado could not be reached for comment.

BEFORE THE GRAND JURY

SITTING FOR THE SOUTHERN DISTRICT OF NEW YORK

‘In re: Sworn Criminal Complaint of
Roderick A. Campbell

SWORN COMPLAINT

I, Roderick A. Campbell, duly swearing to present only
truthful information under penalty to the Grand Jury for the
Southern District of New York, do depose and swear the
following statements of fact and belief as true and accurate to
the best of my knowledge and belief:

3

I am a thoroughly qualified industrial organic
chemist with more than twenty-five (25) years
postgraduate school experience in industry.

I was convicted in February of 1994 in the District of
Rhode island of manufacturing chemical mixtures
said to contain small amounts of P2P and sentenced
in may to serve twenty-four years in prison. |
always contested the presence of any P2P in any of
my mixtures and this was the reason I took trial. At
trial it appeared that 696 grams of mixtures were
contaminated with about 750 parts per million of
P2P while about five kilograms of additional
material was admitted to be negative testing for P2P
to the limits of the scientific methods used, which
was about 1 part per million.

- D.E.A. Chemist Jack Fasanello of the Northeast

Regional D.E.A. Laboratory in Manhattan testified
that he detected P2P in six of the fourteen samples.
He testified that he was the person who received all

of these samples when they arrived at the
laboratory and that he repackaged leaking samples
when required. He also removed the samples from
the custodial vault and performed the testing.

Mr. Fasanello further testified when examined that
all of the positive, and none of the negative, testing
samples arrived at the Northeast Regional’
Laboratory in leading or broken condition.

Mr. Fasanello testified that the first positive testing
sample in the series was established by his analysis
to have been made by a reaction of phenylacetic
acid and acetic anhydride/sodium acetate. I
testified that I had lied to the investigating agent to
say that I would make such a P2P product in that
way, but I also testified that I had admitted to him
that I had lied after he had told me that the sample
had been approved. I never ran the reaction
erroneously reported to Mr. Fasanello, to which his
analysis conforms and this fact is confirmed by the
contemporaneous tape recordings of conversations
made in the investigation.

Long after I was convicted, I learned that the Rhode
Island Laboratory had analyzed all of these same
samples by the same method that had been used by
Mr. Fasanello. This service had been provided
informally to local agents because of the backlog of
work at the D.E.A. Laboratory. I requested copies
of all the work done in Rhode Island pursuantto the
Rhode Island Freedom of Information Act satute.
As a normal precaution, I had all this orginal
information sent to Mr. Albert West, Esq., Manning
and West, Attorneys, 1500 Hospital Trust Tower,
Providence, Rhode Island 02903. Mr. West has
furnished myself and the other parties mentioned in

this Complaint with attested copies of this
information wherever it has been reviewed.

The most glaring discovery from this data for a
layman is the proof that the first positive-testing
sample, which I lied about the method used and the
D.E.A. Laboratory still produced an analysis to
match the unused method, is completely different in
appearance, matching what I say was really done
and exposing Mr. Fasanello's sample and analysis to
be tampered and a lie. The other analyses
performed by the R.I. Dept. of Health Laboratory
consistently show no P2P for all fourteen samples;
there is no chromatogram "peak" at the location
where P2P would appear in any of these analyses.

I have submitted this data, first the naked D.E.A.
data when that was all that I had, and then
supplemented it with the RI. data, to Morris
Forensics, i.e., Mr. Wayne Morris. Mr. Morris wrote
an Affidavit on the quality of the D.E.A. analysis
without knowing of the discrepancy with the
R.L data. I submitted this data to Dr. William Suggs,
a biochemistry research associate professor at
Brown University, who was the retained defense
expert at my trial, who has submitted an Affidavit. |
have also submitted this data through a chemist
who took an interest in my case to the research
departments of Union Carbide Central Research,
B.F. Goodrich Specialty Chemicals, and a division of
Pfizer, Inc. Through the respective research
directors of these research groups I am informed
that the data from the two sources is "irreconcilable"
and that the complete consensus of all the scientists
is that I was framed.

Based on this information I sent a Sworn Criminal
Complaint to the Office of United States Inspector

10.

11.

General in June of this past year. When Dr. Suggs'
Affidavit became available to me in July, I called the
Office Of Inspector General to learn where it should
be sent. I was told that 1 would have to submit a
freedom of information act request for that infor-
mation. That suggestion seemed bizarre, but they
also said I could just send it. So I did. However, in
December, having heard nothing about the
Complaint, I asked Attorney West to check with Dr.
David Uliss, the Director Of Forensic Chemistry of
the R.I. Dept. of Health Laboratory. It was reported
back to me through Mr. West that no one has
-contacted Dr. Uliss or anyone at his laboratory
about my case.

I have just recently read an article from the August 8
issue of "the Nation" that says that the Attorney
General issued an unpublished memorandum order
to the Inspector General in 1994 prohibiting his
office from investigating the D.E.A. and the F.B.I.
Based on this discovery and the fact that the statute
of limitations is nearing closure, I have researched
the subject of a general grand jury investigation and
find that you should investigate this presentation
pursuant to 18 U.S.C. § 3332.

I accuse D.E.A. Chemist Jack Fasanello of
manufacturing controlled mixtures containing P2P
from mixtures that originally contained none. |
accuse Chemist Jack Fasanello of distributing these
controlled substance mixtures to the State of Rhode
Island for my trial. I accuse him of falsifying
evidence, both the samples and the evidence
presented as documentary proof of the analyses;
and I accuse him of perjury in his testimony at my
trial.

12. 1 further swear to any factual statements made in
any of the supporting documents which are
appended to this Complaint as if they were set forth
at length in this Affidavit. | subscribe all the
foregoing once again under penalty of perjury.

Further Your Deponent Sayeth Not,

/s/ 2/4/98
Roderick A. Campbell 03869-070
P.O. Box 759

Minersville, Pennsylvania 17954

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Analyzer temp.: N/A Transfer line temp. : 0
temperetures : 60. 100. 2860. 0. 0.
times, min. 1.5 § 10.0 0.0 0.0
rete, deaq/min: 10.0 15.0 0.0 -5 Cc:
Reject: 5.00 % Mex Peaks: 9? Bunch: 1 Valley »>190 %
ts File VYDIR76 Sorted by Time/Ares INT
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3535 149 7a@76? 4667386 454440 £3.42 >. aR
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203 211 255702 1792214 1740096¢* 59.42 1S. 354
224 227 262458 1723116 1711217 49.78 13.134
256 259 169724 611323 606214 17.63 4.053
288 291 348665 2765249 2756166 60.17 21.155
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357 359 227708 615222 601722 17.50 4.618
461 462 333890 3459979 3437736 100.006 26.384
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2-Prcpeanone, 1l-phenyl- . 134 C9H100
2-Propanone. 1-phenyl- 134 C9H100

Nee

Semple file: +*jC019 Spectrum @#: ‘203
Seerch speed: 2 Tilting option: S No. of 10M ranges searched: a=.
Prob. CAS @ CON ¢ ROOT kK OK @FLG TILT % CON C_I R_Iv
930 103797 31502 “BIGOB 80 5 1 2 88 2 68 80
4 36° 103797 315046 “B1IGDB 60 36 2 1 52 S$ 60 38

MGR

Sample “1” D.E.A.,

|
TIC of CH910001X17. 4
A5299; Run at 08:57 AM EST on Wed Mar 17, 1993
Abundance vp

DIBENZYLKETONE

PHENYLACETIC
3000000 ACID

2000000 =
1000000 <
. . - . = T tT T T T v T T T T . we 7 py
o 6 2

as 7
ae epee wee”

Beginning at 5.33 minutes, the peaks in the D.O.H. analysis

have been identified as 4-chlorobutane-I-acetate, 2- or 3-
methylacetophenone (6.20), 4- methylacetophenone (6.50),
benzylacetate (6.85), unknowns (toluic derivatives suspect),
and bibenzyl (10.81). There may also be brominated
substances. Scan 207, 4-methylacetophenone, was wrongly
identified as P2P in this analysis.

9

CORRESPONDING SAMPLES PFR RAIAIM APFIDAVIT
SAMPLE

23A D.B.A.
ABVEZT I, re _. ae eee Op 21, 1933
)
$.000+07
4800-07
3.900-07
2.900007
1280-87
0200 +09 —Bampnthet Smet AF Beppe ea Sn oun Sen Somme ome oon oe ce ae oe ee
4 ‘ 4 18 12 4
Tene (min.)
a SAMPLE 7A D.O.H.
eee aad eee i 69e wr ope i 19008 a
1900004
= .4a°*
— 1 18.40
600cee
49006,
2000e
Newey - omen
ae ee 3 18 12 14 16 18 20 22

Sample 23A is the most representative sample with complete

data.

---

Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/brief%3Amicro_IA40386015_0397%3A1. Public record. Not legal advice.
