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Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/2522

Title: Orientation and molecular structure of 1,5 and 1,8 dichloroanthraquinones by PMR in a nematic solution
Authors: Sharma, B.B.
Saupe, A.
Khetrapal, C.L.
Kunwar, A.C.
Issue Date: Sep-1983
Publisher: Gordon and Breach Science Publishers.
Citation: Molecular Crystals and Liquid Crystals, 1983, Vol.95, p359-366
Abstract: The structures and the order parameters of 1,5 and 1,8 dichloroanthraquinones have been determined from the dipolar couplings between the protons in the nematic solutions. The results show the effect of steric interactions on the molecular structure. The aromatic rings of 1,8 dichloroanthraquinone are in different planes making an angle of 15° while 1,5 dichlo-roanthraqutnone appears to be flat. The two molecules show peculiar differences in orientation. The "in-plane" order parameters of the 1,8 derivative are about equal while the 1,5 derivative has a strongly preferred alignment axis close to the Cl, Cl internuclear axis.
Description: Restricted Access.
URI: http://hdl.handle.net/2289/2522
ISSN: 1058-725X
Alternative Location: http://dx.doi.org/10.1080/00268948308072475
Copyright: 1983 OPA (Overseas Publishers Association) N.V.
Appears in Collections:Research Papers (SCM)

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