'Ship-in-a-bottle' formation of stable hydrophobic dimers of cis- azobenzene and -stilbene derivatives in a self-assembled coordination nanocage [10]

Journal of the American Chemical Society

Volumn 121, Issue 6, 1999, Pages 1397-1398

  Kusukawa, Takahiro ^a   Fujita, Makoto ^a,b  

^a INSTITUTE FOR MOLECULAR SCIENCE   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AZOBENZENE DERIVATIVE; STILBENE DERIVATIVE;

CHEMICAL BOND; CHEMICAL STRUCTURE; COMPLEX FORMATION; HYDROGEN BOND; ISOMERISM; LETTER; MOLECULAR INTERACTION; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0033576970     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9837295     Document Type: Letter

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29. 3, azobenzene).
30. 2 3.0 package on a Silicon Graphics Octane machine.
31. 3, stilbene).
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33. 2).
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35. It is interesting that trans-5 is not directly enclathrated by 1 but can be enclathrated via isomerization to cis, enclathration, followed by reisomerization to trans.
36. 2).
37. Upon the addition of 1,3,5-trimethoxybenzene to 1, the color of the solution turned yellow immediately and the quantitative formation 1:4 complex was observed. However, strong charge-transfer band was not observed.
38. 2, dibenzyl).