Literature DB >> 25407600

Fullerene cyanation does not always increase electron affinity: an experimental and theoretical study.

Tyler T Clikeman1, Shihu H M Deng, Alexey A Popov, Xue-Bin Wang, Steven H Strauss, Olga V Boltalina.   

Abstract

The electron affinities of C70 derivatives with trifluoromethyl, methyl and cyano groups were studied experimentally and theoretically using low-temperature photoelectron spectroscopy (LT PES) and density functional theory (DFT). The electronic effects of these functional groups were determined and found to be highly dependent on the addition patterns. Substitution of CF3 for CN for the same addition pattern increases the experimental electron affinity by 70 meV per substitution. The synthesis of a new fullerene derivative, C70(CF3)10(CN)2, is reported for the first time.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 25407600     DOI: 10.1039/c4cp04287e

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  1 in total

1.  (19)F NMR-, ESR-, and vis-NIR-spectroelectrochemical study of the unconventional reduction behaviour of a perfluoroalkylated fullerene: dimerization of the C70(CF3)10(-) radical anion.

Authors:  Michal Zalibera; Peter Machata; Tyler T Clikeman; Marco Rosenkranz; Steven H Strauss; Olga V Boltalina; Alexey A Popov
Journal:  Analyst       Date:  2015-11-07       Impact factor: 4.616

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.