Christopher B. Gorman

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Name: Gorman, Christopher B.
Organization: Department of Chemistry North Carolina State University Box 8204 , USA
Department: Department of Chemistry North Carolina State University Box 8204
Title: Professor(PhD)

TOPICS

Co-reporter:Gilbert A. Castillo, Lance Wilson, Kirill Efimenko, Michael D. Dickey, Christopher B. Gorman, and Jan Genzer
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 51) pp:
Publication Date(Web):December 6, 2016
DOI:10.1021/acsami.6b12155
This paper describes surface functionalization of poly(ethylene terephthalate) (PET) films by transamidation of the ester groups with primary amines. The use of water as a solvent improves tremendously the reaction rate and yield compared to conventionally used alcohols. In this study, PET films were exposed to an aqueous solution of 3-aminopropyltriethoxysilane (APTES), which resulted in ester-to-amide reactions on the surface of the film. Hydrolysis of the resulting ethoxy moieties in APTES creates hydroxyl groups that can be used as anchoring points for further modification of PET films. This scheme offers an alternative approach to modify polyesters using water as the solvent.Keywords: 3-aminopropyltriethoxysilane; amidation; APTES; aqueous; PET; poly(ethylene terephthalate); polyester; surface activation; surface modification;
Co-reporter:Yun-Ho Kim and Christopher B. Gorman
Langmuir 2011 Volume 27(Issue 10) pp:6069-6075
Publication Date(Web):April 15, 2011
DOI:10.1021/la2005979
It is shown that self-assembled monolayers (SAMs) composed of α,ω-diynes on gold have different structures depending on the concentration of molecules used to make the SAM. Evidence for both hairpinned and standing-up molecules is provided. This behavior is in contrast to SAMs of α,ω-dithiols on gold, which generally form SAMs with only the straight conformation. The looped SAMs composed of α,ω-diynes offer a less densely packed and thus somewhat accessible surface that may be useful when the underlying surface is used as an electrode. Furthermore, biasing the structure of the molecules in the SAM between looped and standing-up may be useful in the design of dynamic surfaces.
Co-reporter:Eric Z. Tucker and Christopher B. Gorman
Langmuir 2010 Volume 26(Issue 18) pp:15027-15034
Publication Date(Web):August 26, 2010
DOI:10.1021/la101676h
Self-assembled monolayers (SAMs) comprised from n-alkanethiols and terminal alkynes were subjected to solutions containing ferrocene-terminated thiol, thioacetate, and terminal alkyne. The rate and extent of chemical exchange were monitored by scanning tunneling microscopy (STM). In several cases, a rate constant for exchange could be obtained by fitting to a model for exchange. In each case where this could be accomplished, a different rate model gave the best fit to the data, suggesting that the mechanism of exchange depended on either or both the original SAM and the incoming molecule. In scenarios where the rate of exchange was slow, directed exchange was accomplished via STM tip-induced lithographic patterning (replacement lithography). The extent of exchange was independent of the incoming molecule, suggesting that tip-induced desorption was the limiting factor in this process.
Co-reporter:Yanjun Wan, Weijun Niu, William J. Behof, Yifei Wang, Paul Boyle, Christopher B. Gorman
Tetrahedron 2009 65(22) pp: 4293-4297
Publication Date(Web):
DOI:10.1016/j.tet.2009.03.063
Co-reporter:Young-Rae Hong and Christopher B. Gorman  
Chemical Communications 2007 (Issue 30) pp:3195-3197
Publication Date(Web):30 May 2007
DOI:10.1039/B704585A
Here we report the first measurement of homogeneous electron transfer between oxidized and reduced metal tris(bipyridine) core dendrimers by NMR line-broadening; the results indicated that, as the generation of the dendrimer increased, the rate of self-exchange decreased.
Co-reporter:Ronald A. Wassel
Angewandte Chemie International Edition 2004 Volume 43(Issue 39) pp:
Publication Date(Web):16 SEP 2004
DOI:10.1002/anie.200301735

Molecular structure–property relationships for molecular electronics are beginning to emerge. Recent experiments lend credibility to the single-molecule nature of transport measurements and illustrate the molecular features that give rise to various interesting conductance behaviors (see picture).

Co-reporter:Ronald A. Wassel
Angewandte Chemie 2004 Volume 116(Issue 39) pp:
Publication Date(Web):16 SEP 2004
DOI:10.1002/ange.200301735

Struktur-Eigenschafts-Beziehungen sind die Voraussetzung für den Einsatz von Molekülen als Komponenten in der molekularen Elektronik. Kürzlich konnten Einzelmoleküle in Transportmessungen analysiert werden. Die Ergebnisse verdeutlichen das bemerkenswerte Leitfähigkeitsverhalten von Einzelmolekülanordnungen (siehe Bild).

Co-reporter:R.R. Fuierer;R.L. Carroll;D.L. Feldheim;C.B. Gorman
Advanced Materials 2002 Volume 14(Issue 2) pp:
Publication Date(Web):17 JAN 2002
DOI:10.1002/1521-4095(20020116)14:2<154::AID-ADMA154>3.0.CO;2-B
Co-reporter:C.S. Cameron;C.B. Gorman
Advanced Functional Materials 2002 Volume 12(Issue 1) pp:
Publication Date(Web):9 JAN 2002
DOI:10.1002/1616-3028(20020101)12:1<17::AID-ADFM17>3.0.CO;2-V

Dendrimers are potentially useful for encapsulation of core moieties. Although the conformation that a dendrimer assumes around a core moiety cannot be directly determined, the effect of increasing dendrimer size on the photophysical and electrochemical properties of the core has been documented. Specifically, studies of electroactive core dendrimers have shown attenuation of electron transfer rates with increasing dendrimer size, which is an indication of encapsulation. However, in two recent, independent reports of electroactive core dendrimers, electron transfer rates are not attenuated as the dendrimer size increases. These reports illustrate the caution that must be taken when inferring conformation from primary structure in dendritic macromolecules.

Co-reporter:R. Lloyd Carroll Dr.
Angewandte Chemie 2002 Volume 114(Issue 23) pp:
Publication Date(Web):27 NOV 2002
DOI:10.1002/1521-3757(20021202)114:23<4556::AID-ANGE4556>3.0.CO;2-W

Die molekulare Elektronik ist zwar eine noch junge Disziplin, dennoch konnten bereits große Fortschritte erzielt werden, und wir erkennen heute sehr deutlich, welche Materialien geeignet sind und welche Eigenschaften sie aufweisen müssen. Dieser Aufsatz soll auf breiter Basis die derzeit vielversprechendsten Ansätze für eine molekulare Elektronik vorstellen und in ihre Teildisziplinen einführen. Wir behandeln zunächst die historische Entwicklung der konventionellen Elektronik und zeigen auf, welche Faktoren den Beginn der molekularen Elektronik ausgelöst haben. Die Probleme, die bei der Miniaturisierung konventioneller Bauelemente auftreten, werden ebenso diskutiert wie einige Lösungsansätze. Daran anschließend stellen wir die wichtigsten Ergebnisse auf diesem Gebiet vor, die einen tiefen Einblick in das Verhalten molekularer Systeme geben.

Co-reporter:R. Lloyd Carroll Dr.
Angewandte Chemie International Edition 2002 Volume 41(Issue 23) pp:
Publication Date(Web):27 NOV 2002
DOI:10.1002/1521-3773(20021202)41:23<4378::AID-ANIE4378>3.0.CO;2-A

Molecular electronics is, relatively speaking, a young field. Even so, there have been many significant advances and a much greater understanding of the types of materials that will be useful in molecular electronics, and their properties. The purpose of this review is to provide a broad basis for understanding the areas where new advances might arise, and to provide introduction to the subdisciplines of molecular electronics. This review is divided into two major parts; an historical examination of the development of conventional electronics, which should provide some understanding of the push towards molecular electronics. The problems associated with continuing to shrink conventional systems are presented, along with references to some of the efforts to solve them. This section is followed by an in-depth look at the most important research into the types of behaviors that molecular systems have been found to display.

Co-reporter:Christopher Gorman
Nature 2002 415(6871) pp:487
Publication Date(Web):
DOI:10.1038/415487a
Controlled binding of atoms or molecules within a larger structure could offer new routes to drug delivery or nanoscale materials. Synthetic dendrimers can be tailored to bind ions in just such a regulated manner.
Co-reporter:Christopher B. Gorman;Rakesh Sachdeva;Wendy Y. Su;Jennifer C. Smith;Hongwei Jiang
Macromolecular Symposia 2000 Volume 156(Issue 1) pp:61-68
Publication Date(Web):16 MAR 2001
DOI:10.1002/1521-3900(200007)156:1<61::AID-MASY61>3.0.CO;2-7

We are constructing a model system to elucidate the molecular structure-property relationships for attenuation of electron transfer (e.g. electron encapsulation). This information is relevant in bio-electron transfer schemes and in emerging molecular electronics schemes such as storage of information using individual molecules. Our system consists of an inorganic cluster surrounded by dendritic ligands which act as an organic coating. Although the electrochemical and photophysical properties of a variety of metal clusters have been established, very little has been described on the chemistry on metal clusters.

Co-reporter:Young-Rae Hong and Christopher B. Gorman
Chemical Communications 2007(Issue 30) pp:NaN3197-3197
Publication Date(Web):2007/05/30
DOI:10.1039/B704585A
Here we report the first measurement of homogeneous electron transfer between oxidized and reduced metal tris(bipyridine) core dendrimers by NMR line-broadening; the results indicated that, as the generation of the dendrimer increased, the rate of self-exchange decreased.
Co-reporter:Christopher B. Gorman ; Randall J. Petrie ;Jan Genzer
Macromolecules () pp:
Publication Date(Web):June 10, 2008
DOI:10.1021/ma8004857
Poly(methyl methacrylate) (PMMA) anchored chains were grown on porous silicon (p-Si) and anodically etched aluminum oxide (AAO) substrates via surface-initiated atom transfer radical polymerization (ATRP). Using hydrogen fluoride, the chains could be cleaved from the substrates, as evidenced by infrared spectroscopy. The molecular weights and molecular weight distributions of PMMA could be analyzed directly on these substrates (after cleaving the chains from the support) using direct ionization mass spectrometry (DIOS-MS) and matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS). Two principal conclusions were drawn from the study. First, matrix-free DIOS-MS was effective at direct analysis of the polymers up to a molecular weight of ≈6 kDa; the signal-to-noise ratio for heavier polymer chains diminished rapidly. Second, under the same polymerization conditions, PMMA grown on both p-Si and AAO substrates had a much lower molecular weight and a broader molecular weight distribution than that grown in solution. Confinement effects imposed by the pores during the polymerization are proposed as the likely mechanism for the reduced growth rates and more polydisperse chains.
2,2,2-TRIFLUORO-N-(2-OXA-6-AZASPIRO[3.4]OCT-8-YL)ACETAMIDE
Benzamide,N,4-dimethyl-