1,3,5-Triaroylbenzenes as versatile inclusion hosts via C-H...O hydrogen bonding

F. Christopher Pigge; Zhanmiao Zheng; Nigam P. Rath

doi:10.1039/A910190J

1,3,5-Triaroylbenzenes as versatile inclusion hosts via C-H...O hydrogen bonding

F. Christopher Pigge
, Zhanmiao Zheng
, Nigam P. Rath

University of Missouri-St. Louis

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

Original language	American English
Journal	New Journal of Chemistry
Volume	24
DOIs	https://doi.org/10.1039/A910190J
State	Published - Jan 1 2000

Disciplines

Organic Chemistry
Inorganic Chemistry

Access to Document

10.1039/A910190JLicense: Unspecified

Cite this

@article{3a7d193a421e4d02a9683df7b63f7124,

title = "1,3,5-Triaroylbenzenes as versatile inclusion hosts via C-H...O hydrogen bonding",

author = "Pigge, \{F. Christopher\} and Zhanmiao Zheng and Rath, \{Nigam P.\}",

note = "1,3,5-Tris(4-nitrobenzoyl)benzene was prepared by cyclotrimerization of (4-nitrobenzoyl)acetylene. This material was found to form 1:1 crystalline inclusion complexes with CHCl and DMSO as revealed by X-ray crystallography. These inclusion complexes are mediated by C-H···O hydrogen bonding.",

year = "2000",

month = jan,

day = "1",

doi = "10.1039/A910190J",

language = "American English",

volume = "24",

journal = "New Journal of Chemistry",

}

TY - JOUR

T1 - 1,3,5-Triaroylbenzenes as versatile inclusion hosts via C-H...O hydrogen bonding

AU - Pigge, F. Christopher

AU - Zheng, Zhanmiao

AU - Rath, Nigam P.

N1 - 1,3,5-Tris(4-nitrobenzoyl)benzene was prepared by cyclotrimerization of (4-nitrobenzoyl)acetylene. This material was found to form 1:1 crystalline inclusion complexes with CHCl and DMSO as revealed by X-ray crystallography. These inclusion complexes are mediated by C-H···O hydrogen bonding.

PY - 2000/1/1

Y1 - 2000/1/1

UR - http://pubs.rsc.org/en/content/articlelanding/2000/nj/a910190j#!

U2 - 10.1039/A910190J

DO - 10.1039/A910190J

M3 - Article

VL - 24

JO - New Journal of Chemistry

JF - New Journal of Chemistry

ER -

1,3,5-Triaroylbenzenes as versatile inclusion hosts via C-H...O hydrogen bonding

Disciplines

Access to Document

Other files and links

Cite this