Tetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1): A multi-electron donor system subject to conformational control

Atanu Jana; Masatoshi Ishida; Kevin Cho; Sudip Kumar Ghosh; Kyuju Kwak; Kei Ohkubo; Young Mo Sung; Christina M. Davis; Vincent M. Lynch; Dongil Lee; Shunichi Fukuzumi; Dongho Kim; Jonathan L. Sessler

doi:10.1039/c3cc44934c

Tetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1): A multi-electron donor system subject to conformational control

Atanu Jana
, Masatoshi Ishida
, Kevin Cho
, Sudip Kumar Ghosh
, Kyuju Kwak
, Kei Ohkubo
, Young Mo Sung
, Christina M. Davis
, Vincent M. Lynch
, Dongil Lee
, Shunichi Fukuzumi
, Dongho Kim
, Jonathan L. Sessler

Department of Chemistry & Nanoscience

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

13 Scopus citations

Abstract

Tetrathiafulvalenes (TTF)-annulated [28]hexaphyrin affords an electron rich flexible π-conjugated system whose limiting conformations can be controlled through choice of solvents. The conformation-dependent intramolecular charge transfer character, as well as electron reserve capability of the hexakis-TTF annulated hexaphyrin, was analyzed.

Original language	English
Pages (from-to)	8937-8939
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	79
DOIs	https://doi.org/10.1039/c3cc44934c
State	Published - 10 Sep 2013

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title = "Tetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1): A multi-electron donor system subject to conformational control",

abstract = "Tetrathiafulvalenes (TTF)-annulated [28]hexaphyrin affords an electron rich flexible π-conjugated system whose limiting conformations can be controlled through choice of solvents. The conformation-dependent intramolecular charge transfer character, as well as electron reserve capability of the hexakis-TTF annulated hexaphyrin, was analyzed.",

author = "Atanu Jana and Masatoshi Ishida and Kevin Cho and Ghosh, \{Sudip Kumar\} and Kyuju Kwak and Kei Ohkubo and \{Mo Sung\}, Young and Davis, \{Christina M.\} and Lynch, \{Vincent M.\} and Dongil Lee and Shunichi Fukuzumi and Dongho Kim and Sessler, \{Jonathan L.\}",

year = "2013",

month = sep,

day = "10",

doi = "10.1039/c3cc44934c",

language = "English",

volume = "49",

pages = "8937--8939",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "79",

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TY - JOUR

T1 - Tetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1)

T2 - A multi-electron donor system subject to conformational control

AU - Jana, Atanu

AU - Ishida, Masatoshi

AU - Cho, Kevin

AU - Ghosh, Sudip Kumar

AU - Kwak, Kyuju

AU - Ohkubo, Kei

AU - Mo Sung, Young

AU - Davis, Christina M.

AU - Lynch, Vincent M.

AU - Lee, Dongil

AU - Fukuzumi, Shunichi

AU - Kim, Dongho

AU - Sessler, Jonathan L.

PY - 2013/9/10

Y1 - 2013/9/10

N2 - Tetrathiafulvalenes (TTF)-annulated [28]hexaphyrin affords an electron rich flexible π-conjugated system whose limiting conformations can be controlled through choice of solvents. The conformation-dependent intramolecular charge transfer character, as well as electron reserve capability of the hexakis-TTF annulated hexaphyrin, was analyzed.

AB - Tetrathiafulvalenes (TTF)-annulated [28]hexaphyrin affords an electron rich flexible π-conjugated system whose limiting conformations can be controlled through choice of solvents. The conformation-dependent intramolecular charge transfer character, as well as electron reserve capability of the hexakis-TTF annulated hexaphyrin, was analyzed.

UR - https://www.scopus.com/pages/publications/84883879864

U2 - 10.1039/c3cc44934c

DO - 10.1039/c3cc44934c

M3 - Article

C2 - 23970175

AN - SCOPUS:84883879864

SN - 1359-7345

VL - 49

SP - 8937

EP - 8939

JO - Chemical Communications

JF - Chemical Communications

IS - 79

ER -

Tetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1): A multi-electron donor system subject to conformational control

Abstract

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