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,

day = "26",

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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