Molecular recognition: designed crystalline inclusion complexes of carboxylic hosts

1989 ◽  
Vol 7 (1) ◽  
pp. 12-27 ◽  
Author(s):  
Edwin Weber
RSC Advances ◽  
2021 ◽  
Vol 11 (22) ◽  
pp. 13091-13096
Author(s):  
Lu Chen ◽  
Yanbin Huang

Guest polymers have significant influence on the dissolution of drug–polymer inclusion complex crystals.


2002 ◽  
Vol 35 (9) ◽  
pp. 3778-3780 ◽  
Author(s):  
Xintao Shuai ◽  
Francis E. Porbeni ◽  
Min Wei ◽  
Todd Bullions ◽  
Alan E. Tonelli

2007 ◽  
Vol 48 (3) ◽  
pp. 540-546 ◽  
Author(s):  
O. V. Andreeva ◽  
B. F. Garifullin ◽  
A. T. Gubaidullin ◽  
V. A. Al’fonsov ◽  
V. E. Kataev ◽  
...  

2008 ◽  
pp. 4726 ◽  
Author(s):  
F. Christopher Pigge ◽  
Venu R. Vangala ◽  
Pradeep P. Kapadia ◽  
Dale C. Swenson ◽  
Nigam P. Rath

Pharmaceutics ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 60
Author(s):  
Borja Gómez-González ◽  
Luis García-Río ◽  
Nuno Basílio ◽  
Juan C. Mejuto ◽  
Jesus Simal-Gandara

The formation of inclusion complexes between alkylsulfonate guests and a cationic pillar[5]arene receptor in water was investigated by NMR and ITC techniques. The results show the formation of host-guest complexes stabilized by electrostatic interactions and hydrophobic effects with binding constants of up to 107 M−1 for the guest with higher hydrophobic character. Structurally, the alkyl chain of the guest is included in the hydrophobic aromatic cavity of the macrocycle while the sulfonate groups are held in the multicationic portal by ionic interactions.


Chirality ◽  
1989 ◽  
Vol 1 (2) ◽  
pp. 137-141 ◽  
Author(s):  
Heng L. Jin ◽  
Apryll Stalcup ◽  
Daniel W. Armstrong

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