Pyrene-fused subphthalocyanine

Soji Shimizu; Shota Nakano; Takahisa Hosoya; Nagao Kobayashi

doi:10.1039/c0cc01877e

Pyrene-fused subphthalocyanine

Soji Shimizu, Shota Nakano, Takahisa Hosoya, Nagao Kobayashi

SCI - Chemistry

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

60 Citations (Scopus)

Abstract

A pyrene-fused subphthalocyanine synthesized from a reaction of 2,7-di-tert-butyl-4,5,9,10-tetracyanopyrene and tetrafluorophthalonitrile exhibits red-shifted Q-band absorption and a unique linear arrangement in the solid state caused by a π-π stacking interaction. The concave conjugation of the SubPc moiety and the planar conjugation of the pyrene moiety enhanced its co-crystallization with C₆₀ molecules.

Original language	English
Pages (from-to)	316-318
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	1
DOIs	https://doi.org/10.1039/c0cc01877e
Publication status	Published - 2011 Jan 7

ASJC Scopus subject areas

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

Access to Document

10.1039/c0cc01877e

Cite this

@article{cf601949069c444e8b3b2c7d90c21ebc,

title = "Pyrene-fused subphthalocyanine",

abstract = "A pyrene-fused subphthalocyanine synthesized from a reaction of 2,7-di-tert-butyl-4,5,9,10-tetracyanopyrene and tetrafluorophthalonitrile exhibits red-shifted Q-band absorption and a unique linear arrangement in the solid state caused by a π-π stacking interaction. The concave conjugation of the SubPc moiety and the planar conjugation of the pyrene moiety enhanced its co-crystallization with C60 molecules.",

author = "Soji Shimizu and Shota Nakano and Takahisa Hosoya and Nagao Kobayashi",

year = "2011",

month = jan,

day = "7",

doi = "10.1039/c0cc01877e",

language = "English",

volume = "47",

pages = "316--318",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "1",

}

TY - JOUR

T1 - Pyrene-fused subphthalocyanine

AU - Shimizu, Soji

AU - Nakano, Shota

AU - Hosoya, Takahisa

AU - Kobayashi, Nagao

PY - 2011/1/7

Y1 - 2011/1/7

N2 - A pyrene-fused subphthalocyanine synthesized from a reaction of 2,7-di-tert-butyl-4,5,9,10-tetracyanopyrene and tetrafluorophthalonitrile exhibits red-shifted Q-band absorption and a unique linear arrangement in the solid state caused by a π-π stacking interaction. The concave conjugation of the SubPc moiety and the planar conjugation of the pyrene moiety enhanced its co-crystallization with C60 molecules.

AB - A pyrene-fused subphthalocyanine synthesized from a reaction of 2,7-di-tert-butyl-4,5,9,10-tetracyanopyrene and tetrafluorophthalonitrile exhibits red-shifted Q-band absorption and a unique linear arrangement in the solid state caused by a π-π stacking interaction. The concave conjugation of the SubPc moiety and the planar conjugation of the pyrene moiety enhanced its co-crystallization with C60 molecules.

UR - http://www.scopus.com/inward/record.url?scp=78649817482&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=78649817482&partnerID=8YFLogxK

U2 - 10.1039/c0cc01877e

DO - 10.1039/c0cc01877e

M3 - Article

C2 - 20730176

AN - SCOPUS:78649817482

SN - 1359-7345

VL - 47

SP - 316

EP - 318

JO - Chemical Communications

JF - Chemical Communications

IS - 1

ER -

Pyrene-fused subphthalocyanine

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this