Similar but Not the Same: Difference in the Ability to Form Cocrystals between Nimesulide and the Pyridine Analogues-Reference-Cited by-同舟云学术

Similar but Not the Same: Difference in the Ability to Form Cocrystals between Nimesulide and the Pyridine Analogues

Published:2020-11-20 Issue:1 Volume:21 Page:287-296
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Wang Mengwei¹,Ma Yiming¹,Shi Peng¹,Du Shichao¹^ORCID,Wu Songgu¹^ORCID,Gong Junbo¹²^ORCID

Affiliation:

1. State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, People’s Republic of China

2. Key Laboratory Modern Drug Delivery and High Efficiency in Tianjin, Tianjin, People’s Republic of China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.cgd.0c01132

Reference39 articles.

1. Three Energetic 2,2′,4,4′,6,6′-Hexanitrostilbene Cocrystals Regularly Constructed by H-bonding, π-Stacking, and van der Waals Interactions

2. π–π Stacking Contributing to the Low or Reduced Impact Sensitivity of Energetic Materials

3. Rapid Cocrystallization by Exploiting Differential Solubility: An Efficient and Scalable Process toward Easily Fabricating Energetic Cocrystals

4. An organic–inorganic hybrid co-crystal complex as a high-performance solid-state nonlinear optical switch

5. Cocrystals of 2-Aminopyrimidine with Boric Acid—Crystal Engineering of a Novel Nonlinear Optically (NLO) Active Crystal

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