Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction

Brittni A. Qualizza; Srividya Prasad; M. Paul Chiarelli; Jacob W. Ciszek

doi:10.1039/c3cc40866c

Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction

Brittni A. Qualizza
, Srividya Prasad
, M. Paul Chiarelli
, Jacob W. Ciszek

Department of Chemistry and Biochemistry

Loyola University Chicago

Research output: Contribution to journal › Article › peer-review

Abstract

A surface adlayer is generated on organic single crystals (tetracene and rubrene) using the site specific Diels–Alder reaction and a series of vapor phase dienophiles. X-ray photoelectron spectroscopy (XPS) confirms adsorption on the surfaces of tetracene and rubrene and mass spectrometry demonstrates the reaction’s applicability to a range of dienophiles.

Original language	American English
Journal	Chemistry: Faculty Publications and Other Works
Volume	49
Issue number	40
DOIs	https://doi.org/10.1039/c3cc40866c
State	Published - Mar 26 2013

Keywords

organic semiconductor crystals
Diels-Alder reaction
crystals
crystallization

Disciplines

Chemistry

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Functionalization of Organic Semiconductor Crystals via the DielsFinal published version, 1.02 MBLicense: Unspecified

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title = "Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction",

abstract = " A surface adlayer is generated on organic single crystals (tetracene and rubrene) using the site specific Diels–Alder reaction and a series of vapor phase dienophiles. X-ray photoelectron spectroscopy (XPS) confirms adsorption on the surfaces of tetracene and rubrene and mass spectrometry demonstrates the reaction{\textquoteright}s applicability to a range of dienophiles.",

keywords = "organic semiconductor crystals, Diels-Alder reaction, crystals, crystallization",

author = "Qualizza, \{Brittni A.\} and Srividya Prasad and Chiarelli, \{M. Paul\} and Ciszek, \{Jacob W.\}",

note = "Qualizza, Brittni A., Srividya Prasad, M. Paul Chiarelli, and Jacob W. Ciszek. {"}Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction.{"} Chemical Communications, 49(40), 2013, http://dx.doi.org/10.1039/C3CC40866C.",

year = "2013",

month = mar,

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doi = "10.1039/c3cc40866c",

language = "American English",

volume = "49",

journal = "Chemistry: Faculty Publications and Other Works",

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TY - JOUR

T1 - Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction

AU - Qualizza, Brittni A.

AU - Prasad, Srividya

AU - Chiarelli, M. Paul

AU - Ciszek, Jacob W.

N1 - Qualizza, Brittni A., Srividya Prasad, M. Paul Chiarelli, and Jacob W. Ciszek. "Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction." Chemical Communications, 49(40), 2013, http://dx.doi.org/10.1039/C3CC40866C.

PY - 2013/3/26

Y1 - 2013/3/26

N2 - A surface adlayer is generated on organic single crystals (tetracene and rubrene) using the site specific Diels–Alder reaction and a series of vapor phase dienophiles. X-ray photoelectron spectroscopy (XPS) confirms adsorption on the surfaces of tetracene and rubrene and mass spectrometry demonstrates the reaction’s applicability to a range of dienophiles.

AB - A surface adlayer is generated on organic single crystals (tetracene and rubrene) using the site specific Diels–Alder reaction and a series of vapor phase dienophiles. X-ray photoelectron spectroscopy (XPS) confirms adsorption on the surfaces of tetracene and rubrene and mass spectrometry demonstrates the reaction’s applicability to a range of dienophiles.

KW - organic semiconductor crystals

KW - Diels-Alder reaction

KW - crystals

KW - crystallization

UR - https://ecommons.luc.edu/chemistry_facpubs/78

UR - https://ecommons.luc.edu/chemistry_facpubs/74

U2 - 10.1039/c3cc40866c

DO - 10.1039/c3cc40866c

M3 - Article

VL - 49

JO - Chemistry: Faculty Publications and Other Works

JF - Chemistry: Faculty Publications and Other Works

IS - 40

ER -

Functionalization of Organic Semiconductor Crystals via the Diels–Alder Reaction

Abstract

Keywords

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