Peripherally ethynylated carbazole-based core-modified porphyrins

Chihiro Maeda; Naoki Yoshioka

doi:10.1039/c2ob25645b

Peripherally ethynylated carbazole-based core-modified porphyrins

Chihiro Maeda, Naoki Yoshioka

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

13 Citations (Scopus)

Abstract

Peripherally ethynylated carbazole-based core-modified porphyrins were synthesized by sequential metal-catalyzed coupling and annulation reactions. Experimental results and DFT calculations both confirm that the π-conjugated networks of the resulting porphyrins effectively delocalize over the entire macrocycle, including the ethynyl substituent groups.

Original language	English
Pages (from-to)	5182-5185
Number of pages	4
Journal	Organic and Biomolecular Chemistry
Volume	10
Issue number	27
DOIs	https://doi.org/10.1039/c2ob25645b
Publication status	Published - Jul 21 2012
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

Access to Document

10.1039/c2ob25645b

Cite this

@article{fa9a340fc126482e9df33e79e37b96f2,

title = "Peripherally ethynylated carbazole-based core-modified porphyrins",

abstract = "Peripherally ethynylated carbazole-based core-modified porphyrins were synthesized by sequential metal-catalyzed coupling and annulation reactions. Experimental results and DFT calculations both confirm that the π-conjugated networks of the resulting porphyrins effectively delocalize over the entire macrocycle, including the ethynyl substituent groups.",

author = "Chihiro Maeda and Naoki Yoshioka",

year = "2012",

month = jul,

day = "21",

doi = "10.1039/c2ob25645b",

language = "English",

volume = "10",

pages = "5182--5185",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "27",

}

TY - JOUR

T1 - Peripherally ethynylated carbazole-based core-modified porphyrins

AU - Maeda, Chihiro

AU - Yoshioka, Naoki

PY - 2012/7/21

Y1 - 2012/7/21

N2 - Peripherally ethynylated carbazole-based core-modified porphyrins were synthesized by sequential metal-catalyzed coupling and annulation reactions. Experimental results and DFT calculations both confirm that the π-conjugated networks of the resulting porphyrins effectively delocalize over the entire macrocycle, including the ethynyl substituent groups.

AB - Peripherally ethynylated carbazole-based core-modified porphyrins were synthesized by sequential metal-catalyzed coupling and annulation reactions. Experimental results and DFT calculations both confirm that the π-conjugated networks of the resulting porphyrins effectively delocalize over the entire macrocycle, including the ethynyl substituent groups.

UR - http://www.scopus.com/inward/record.url?scp=84862841149&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84862841149&partnerID=8YFLogxK

U2 - 10.1039/c2ob25645b

DO - 10.1039/c2ob25645b

M3 - Article

C2 - 22596077

AN - SCOPUS:84862841149

VL - 10

SP - 5182

EP - 5185

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 27

ER -

Peripherally ethynylated carbazole-based core-modified porphyrins

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this