A bis(disulfide)-linked offset cryptophane

Marc A. Little; Malcolm A. Halcrow; Michaele J. Hardie

doi:10.1039/c3cc38768b

A bis(disulfide)-linked offset cryptophane

Marc A. Little, Malcolm A. Halcrow, Michaele J. Hardie^*

^*Corresponding author for this work

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

8 Citations (Scopus)

Abstract

A new bis(disulfide)-linked offset dimer is formed from a dithiolated analogue of cyclotriguaiacylene. Unlike a similar tris(disulfide)-linked example, this is not a true cryptophane as the offset nature of the dimerisation and intramolecular host–guest interactions preclude its use as a host.

Original language	English
Pages (from-to)	1512-1514
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	15
DOIs	https://doi.org/10.1039/c3cc38768b
Publication status	Published - 21 Feb 2013

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/c3cc38768b

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title = "A bis(disulfide)-linked offset cryptophane",

abstract = "A new bis(disulfide)-linked offset dimer is formed from a dithiolated analogue of cyclotriguaiacylene. Unlike a similar tris(disulfide)-linked example, this is not a true cryptophane as the offset nature of the dimerisation and intramolecular host–guest interactions preclude its use as a host.",

author = "Little, \{Marc A.\} and Halcrow, \{Malcolm A.\} and Hardie, \{Michaele J.\}",

year = "2013",

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T1 - A bis(disulfide)-linked offset cryptophane

AU - Little, Marc A.

AU - Halcrow, Malcolm A.

AU - Hardie, Michaele J.

PY - 2013/2/21

Y1 - 2013/2/21

N2 - A new bis(disulfide)-linked offset dimer is formed from a dithiolated analogue of cyclotriguaiacylene. Unlike a similar tris(disulfide)-linked example, this is not a true cryptophane as the offset nature of the dimerisation and intramolecular host–guest interactions preclude its use as a host.

AB - A new bis(disulfide)-linked offset dimer is formed from a dithiolated analogue of cyclotriguaiacylene. Unlike a similar tris(disulfide)-linked example, this is not a true cryptophane as the offset nature of the dimerisation and intramolecular host–guest interactions preclude its use as a host.

UR - https://www.scopus.com/pages/publications/84873036576

U2 - 10.1039/c3cc38768b

DO - 10.1039/c3cc38768b

M3 - Article

AN - SCOPUS:84873036576

SN - 1359-7345

VL - 49

SP - 1512

EP - 1514

JO - Chemical Communications

JF - Chemical Communications

IS - 15

ER -

A bis(disulfide)-linked offset cryptophane

Abstract

ASJC Scopus subject areas

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