Macrocyclic Amphiphiles. 1. Properties of Calix[4]resorcinarene Derivatives Substituted with Azobenzenes in Solutions and Monolayers-Reference-Cited by-同舟云学术

Macrocyclic Amphiphiles. 1. Properties of Calix[4]resorcinarene Derivatives Substituted with Azobenzenes in Solutions and Monolayers

Published:1997-12-01 Issue:25 Volume:13 Page:6780-6786
ISSN:0743-7463
Container-title:Langmuir
language:en
Short-container-title:Langmuir

Author:

Ichimura Kunihiro¹,Fukushima Noriaki¹,Fujimaki Masanori¹,Kawahara Sumie¹,Matsuzawa Yoko¹,Hayashi Yuko¹,Kudo Kazuaki¹

Affiliation:

1. Research Laboratory of Resources Utilization, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226, Japan, and Institute of Industrial Science, University of Tokyo, 7-22-1 Roppongi, Minato-ku, Tokyo 106, Japan

Publisher

American Chemical Society (ACS)

Subject

Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science

Link

https://pubs.acs.org/doi/pdf/10.1021/la970701i

Reference22 articles.

1. Cyclooligomeric phenol-aldehyde condensation products. 2. Stereoselective synthesis and DNMR study of two 1,8,15,22-tetraphenyl[14]metacyclophan-3,5,10,12,17,19,24,26-octols

2. Molecular recognition. 5. Molecular recognition of sugars via hydrogen-bonding interaction with a synthetic polyhydroxy macrocycle

3. Molecular recognition. 8. Two-point hydrogen-bonding interaction: a remarkable chain-length selectivity in the binding of dicarboxylic acids with resorcinol-aldehyde cyclotetramer as a multidentate host

4. Molecular recognition. 15. Molecular recognition and stereoselectivity: geometrical requirements for the multiple hydrogen-bonding interaction of diols with a multidentate polyhydroxy macrocycle

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