Synthesis and properties of acetylene-bridged N-confused porphyrin dimers

Motoki Toganoh; Takumi Takayama; Nandy Ritesh; Nobuo Kimizuka; Hiroyuki Furuta

doi:10.1246/cl.2011.1021

Synthesis and properties of acetylene-bridged N-confused porphyrin dimers

Motoki Toganoh, Takumi Takayama, Nandy Ritesh, Nobuo Kimizuka, Hiroyuki Furuta

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

14 Citations (Scopus)

Abstract

Acetylene-bridged N-confused porphyrin (NCP) dimers were synthesized by Stille coupling reactions. Moderate electronic interaction between the NCP chromophores was observed in the inner-3H tautomers while strong interaction was observed in the inner-2H tautomers.

Original language	English
Pages (from-to)	1021-1023
Number of pages	3
Journal	Chemistry Letters
Volume	40
Issue number	9
DOIs	https://doi.org/10.1246/cl.2011.1021
Publication status	Published - 2011

All Science Journal Classification (ASJC) codes

Chemistry(all)

Access to Document

10.1246/cl.2011.1021

Cite this

@article{262f79bad1ca4a0bbf885847feb02787,

title = "Synthesis and properties of acetylene-bridged N-confused porphyrin dimers",

abstract = "Acetylene-bridged N-confused porphyrin (NCP) dimers were synthesized by Stille coupling reactions. Moderate electronic interaction between the NCP chromophores was observed in the inner-3H tautomers while strong interaction was observed in the inner-2H tautomers.",

author = "Motoki Toganoh and Takumi Takayama and Nandy Ritesh and Nobuo Kimizuka and Hiroyuki Furuta",

year = "2011",

doi = "10.1246/cl.2011.1021",

language = "English",

volume = "40",

pages = "1021--1023",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "The Chemical Society of Japan",

number = "9",

}

TY - JOUR

T1 - Synthesis and properties of acetylene-bridged N-confused porphyrin dimers

AU - Toganoh, Motoki

AU - Takayama, Takumi

AU - Ritesh, Nandy

AU - Kimizuka, Nobuo

AU - Furuta, Hiroyuki

PY - 2011

Y1 - 2011

N2 - Acetylene-bridged N-confused porphyrin (NCP) dimers were synthesized by Stille coupling reactions. Moderate electronic interaction between the NCP chromophores was observed in the inner-3H tautomers while strong interaction was observed in the inner-2H tautomers.

AB - Acetylene-bridged N-confused porphyrin (NCP) dimers were synthesized by Stille coupling reactions. Moderate electronic interaction between the NCP chromophores was observed in the inner-3H tautomers while strong interaction was observed in the inner-2H tautomers.

UR - http://www.scopus.com/inward/record.url?scp=80052594447&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=80052594447&partnerID=8YFLogxK

U2 - 10.1246/cl.2011.1021

DO - 10.1246/cl.2011.1021

M3 - Article

AN - SCOPUS:80052594447

SN - 0366-7022

VL - 40

SP - 1021

EP - 1023

JO - Chemistry Letters

JF - Chemistry Letters

IS - 9

ER -

Synthesis and properties of acetylene-bridged N-confused porphyrin dimers

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this