Open Access. Powered by Scholars. Published by Universities.®
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 2 of 2
Full-Text Articles in Physical Sciences and Mathematics
Functionalization Of Organic Semiconductor Crystals Via The Diels–Alder Reaction, Brittni A. Qualizza, Srividya Prasad, M. Paul Chiarelli, Jacob W. Ciszek
Functionalization Of Organic Semiconductor Crystals Via The Diels–Alder Reaction, Brittni A. Qualizza, Srividya Prasad, M. Paul Chiarelli, Jacob W. Ciszek
Chemistry: Faculty Publications and Other Works
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.
Functionalization Of Organic Semiconductor Crystals Via The Diels-Alder Reaction, Brittni A. Qualizza, Srividya Prasad, M. Paul Chiarelli, Jacob W. Ciszek
Functionalization Of Organic Semiconductor Crystals Via The Diels-Alder Reaction, Brittni A. Qualizza, Srividya Prasad, M. Paul Chiarelli, Jacob W. Ciszek
Chemistry: Faculty Publications and Other Works
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.