Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes

Soji Shimizu; Akito Miura; Nagao Kobayashi

doi:10.1039/c2ce26618k

Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes

Soji Shimizu, Akito Miura, Nagao Kobayashi

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

7 Citations (Scopus)

Abstract

1:1 co-crystallization of phthalocyanine with pristine C₆₀ or C₇₀ was achieved for the first time using a highly deformed phthalocyanine bearing phenyl substituents at α-positions. In the molecular packing diagrams of both cocrystallates, fullerene and phthalocyanine molecules are alternately arranged to form a one-dimensional array.

Original language	English
Pages (from-to)	3759-3762
Number of pages	4
Journal	CrystEngComm
Volume	15
Issue number	19
DOIs	https://doi.org/10.1039/c2ce26618k
Publication status	Published - May 21 2013
Externally published	Yes

All Science Journal Classification (ASJC) codes

Chemistry(all)
Materials Science(all)
Condensed Matter Physics

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10.1039/c2ce26618k

Cite this

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title = "Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes",

abstract = "1:1 co-crystallization of phthalocyanine with pristine C60 or C70 was achieved for the first time using a highly deformed phthalocyanine bearing phenyl substituents at α-positions. In the molecular packing diagrams of both cocrystallates, fullerene and phthalocyanine molecules are alternately arranged to form a one-dimensional array.",

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AU - Miura, Akito

AU - Kobayashi, Nagao

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AB - 1:1 co-crystallization of phthalocyanine with pristine C60 or C70 was achieved for the first time using a highly deformed phthalocyanine bearing phenyl substituents at α-positions. In the molecular packing diagrams of both cocrystallates, fullerene and phthalocyanine molecules are alternately arranged to form a one-dimensional array.

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Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes

Abstract

All Science Journal Classification (ASJC) codes

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