An organogel system can control the stereochemical course of anthracene photodimerization

Arnab Dawn, Norifumi Fujita, Shuichi Haraguchi, Kazuki Sada, Seiji Shinkai

Research output: Contribution to journalArticle

78 Citations (Scopus)

Abstract

A novel photoresponsive organogel with a binary gelator containing 2-anthracenecarboxylic acid shows a high degree of stereochemical control, resulting in head-to-head photocyclodimers exclusively together with significant enantiomeric excess induced by the chiral counterpart of the gelator.

Original languageEnglish
Pages (from-to)2100-2102
Number of pages3
JournalChemical Communications
Issue number16
DOIs
Publication statusPublished - Apr 20 2009

Fingerprint

Anthracene
Control systems
Acids
anthracene-1-carboxylic acid
anthracene

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

An organogel system can control the stereochemical course of anthracene photodimerization. / Dawn, Arnab; Fujita, Norifumi; Haraguchi, Shuichi; Sada, Kazuki; Shinkai, Seiji.

In: Chemical Communications, No. 16, 20.04.2009, p. 2100-2102.

Research output: Contribution to journalArticle

Dawn, Arnab ; Fujita, Norifumi ; Haraguchi, Shuichi ; Sada, Kazuki ; Shinkai, Seiji. / An organogel system can control the stereochemical course of anthracene photodimerization. In: Chemical Communications. 2009 ; No. 16. pp. 2100-2102.
@article{6fbfb16cbb8c424d8fca615142f2b884,
title = "An organogel system can control the stereochemical course of anthracene photodimerization",
abstract = "A novel photoresponsive organogel with a binary gelator containing 2-anthracenecarboxylic acid shows a high degree of stereochemical control, resulting in head-to-head photocyclodimers exclusively together with significant enantiomeric excess induced by the chiral counterpart of the gelator.",
author = "Arnab Dawn and Norifumi Fujita and Shuichi Haraguchi and Kazuki Sada and Seiji Shinkai",
year = "2009",
month = "4",
day = "20",
doi = "10.1039/b820565e",
language = "English",
pages = "2100--2102",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "16",

}

TY - JOUR

T1 - An organogel system can control the stereochemical course of anthracene photodimerization

AU - Dawn, Arnab

AU - Fujita, Norifumi

AU - Haraguchi, Shuichi

AU - Sada, Kazuki

AU - Shinkai, Seiji

PY - 2009/4/20

Y1 - 2009/4/20

N2 - A novel photoresponsive organogel with a binary gelator containing 2-anthracenecarboxylic acid shows a high degree of stereochemical control, resulting in head-to-head photocyclodimers exclusively together with significant enantiomeric excess induced by the chiral counterpart of the gelator.

AB - A novel photoresponsive organogel with a binary gelator containing 2-anthracenecarboxylic acid shows a high degree of stereochemical control, resulting in head-to-head photocyclodimers exclusively together with significant enantiomeric excess induced by the chiral counterpart of the gelator.

UR - http://www.scopus.com/inward/record.url?scp=64549138094&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=64549138094&partnerID=8YFLogxK

U2 - 10.1039/b820565e

DO - 10.1039/b820565e

M3 - Article

C2 - 19360159

AN - SCOPUS:64549138094

SP - 2100

EP - 2102

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 16

ER -