Pseudopolymorphism and Polymorphic Transition Behavior of N-(4′-Methoxyphenyl)-2-naphthalenesulfonamide-Reference-Cited by-同舟云学术

Pseudopolymorphism and Polymorphic Transition Behavior of N-(4′-Methoxyphenyl)-2-naphthalenesulfonamide

Published:2012-12-18 Issue:1 Volume:13 Page:308-314
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Sakai Takahiro¹,Katagiri Kosuke¹,Uemura Yuki¹,Masu Hyuma²,Tominaga Masahide¹,Azumaya Isao¹

Affiliation:

1. Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University, 1314-1 Shido, Sanuki, Kagawa 769-2193, Japan

2. Chemical Analysis Center, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba-city, Chiba 263-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cg301457v

Reference56 articles.

1. aMcCrone, W. C.Physics and Chemistry of the Organic Solid State;Fox, D., Labes, M. M., Weissberger, A., Eds.Wiley Interscience:New York, 1965; Vol.2, pp725–767.

2. bBernstein, J.Organic Solid State Chemistry;Desiraju, G. R., Ed.Elsevier:Amsterdam, 1987; pp471–518.

3. Disappearing Polymorphs

4. When is a polymorph not a polymorph? Helical trimeric O–H···O synthons in trans-1,4-diethynylcyclohexane-1,4-diol

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