Doubly N-confused pentaphyrins

Alagar Srinivasan, Tomoya Ishizuka, Hiromitsu Maeda, Hiroyuki Furuta

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Adding to the confusion: [3+2] coupling of confused tripyrrane and confused dipyrromethane dicarbinol, followed by oxidation, results in the synthesis of mesopentafluorophenyl-substituted, doubly N-confused, oxo-substituted pentaphyrins (see X-ray crystal structure; green: F, blue: N, red: O). The oxopyrrole moieties have been shown to readily form intra- and intermolecular hydrogen bonds.

Original languageEnglish
Pages (from-to)2951-2955
Number of pages5
JournalAngewandte Chemie - International Edition
Volume43
Issue number22
DOIs
Publication statusPublished - May 24 2004

Fingerprint

Hydrogen bonds
Crystal structure
X rays
Oxidation
dipyrromethane

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)

Cite this

Doubly N-confused pentaphyrins. / Srinivasan, Alagar; Ishizuka, Tomoya; Maeda, Hiromitsu; Furuta, Hiroyuki.

In: Angewandte Chemie - International Edition, Vol. 43, No. 22, 24.05.2004, p. 2951-2955.

Research output: Contribution to journalArticle

Srinivasan, A, Ishizuka, T, Maeda, H & Furuta, H 2004, 'Doubly N-confused pentaphyrins', Angewandte Chemie - International Edition, vol. 43, no. 22, pp. 2951-2955. https://doi.org/10.1002/anie.200453732
Srinivasan, Alagar ; Ishizuka, Tomoya ; Maeda, Hiromitsu ; Furuta, Hiroyuki. / Doubly N-confused pentaphyrins. In: Angewandte Chemie - International Edition. 2004 ; Vol. 43, No. 22. pp. 2951-2955.
@article{c4586cc1093c46fb9d8e508a427a45e5,
title = "Doubly N-confused pentaphyrins",
abstract = "Adding to the confusion: [3+2] coupling of confused tripyrrane and confused dipyrromethane dicarbinol, followed by oxidation, results in the synthesis of mesopentafluorophenyl-substituted, doubly N-confused, oxo-substituted pentaphyrins (see X-ray crystal structure; green: F, blue: N, red: O). The oxopyrrole moieties have been shown to readily form intra- and intermolecular hydrogen bonds.",
author = "Alagar Srinivasan and Tomoya Ishizuka and Hiromitsu Maeda and Hiroyuki Furuta",
year = "2004",
month = "5",
day = "24",
doi = "10.1002/anie.200453732",
language = "English",
volume = "43",
pages = "2951--2955",
journal = "Angewandte Chemie - International Edition",
issn = "1433-7851",
publisher = "John Wiley and Sons Ltd",
number = "22",

}

TY - JOUR

T1 - Doubly N-confused pentaphyrins

AU - Srinivasan, Alagar

AU - Ishizuka, Tomoya

AU - Maeda, Hiromitsu

AU - Furuta, Hiroyuki

PY - 2004/5/24

Y1 - 2004/5/24

N2 - Adding to the confusion: [3+2] coupling of confused tripyrrane and confused dipyrromethane dicarbinol, followed by oxidation, results in the synthesis of mesopentafluorophenyl-substituted, doubly N-confused, oxo-substituted pentaphyrins (see X-ray crystal structure; green: F, blue: N, red: O). The oxopyrrole moieties have been shown to readily form intra- and intermolecular hydrogen bonds.

AB - Adding to the confusion: [3+2] coupling of confused tripyrrane and confused dipyrromethane dicarbinol, followed by oxidation, results in the synthesis of mesopentafluorophenyl-substituted, doubly N-confused, oxo-substituted pentaphyrins (see X-ray crystal structure; green: F, blue: N, red: O). The oxopyrrole moieties have been shown to readily form intra- and intermolecular hydrogen bonds.

UR - http://www.scopus.com/inward/record.url?scp=4544358746&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=4544358746&partnerID=8YFLogxK

U2 - 10.1002/anie.200453732

DO - 10.1002/anie.200453732

M3 - Article

C2 - 15170313

AN - SCOPUS:4544358746

VL - 43

SP - 2951

EP - 2955

JO - Angewandte Chemie - International Edition

JF - Angewandte Chemie - International Edition

SN - 1433-7851

IS - 22

ER -