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Volumn 6, Issue 13, 2000, Pages 2462-2469

Stilbenoid dendrimers

Author keywords

Aggregation; Dendrimers; Liquid crystals; Protecting groups; Wittig Horner reactions

Indexed keywords

DENDRIMER; STILBENE DERIVATIVE;

EID: 0034600892     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20000703)6:13<2462::AID-CHEM2462>3.0.CO;2-A     Document Type: Article
Times cited : (119)

References (30)
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    • 5b where the raw product resisted a complete purification. Toluene, in particular, was so strongly captured in the cavities of the dendrimer that it could not be totally removed in the vacuum. See also [16]
    • 5b where the raw product resisted a complete purification. Toluene, in particular, was so strongly captured in the cavities of the dendrimer that it could not be totally removed in the vacuum. See also [16].
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    • The desorbed ion contains two molecules toluene.
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    • A second, independent proof of the aggregation was found with the concentration-dependent emission spectra. The photophysics and the photochemistry of the stilbenoid dendrimers will be discussed elsewhere
    • A second, independent proof of the aggregation was found with the concentration-dependent emission spectra. The photophysics and the photochemistry of the stilbenoid dendrimers will be discussed elsewhere.
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    • Originally, a highly viscous LC phase was found. However, a carefully purified compound, which was stored in the dark, generated a crystalline state in this temperature range. Small amounts of photo-products induce a liquid crystalline phase.
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    • NOE measurements revealed that the inner olefinic protons are shifted to higher fields compared to the outer olefinic protons
    • NOE measurements revealed that the inner olefinic protons are shifted to higher fields compared to the outer olefinic protons.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.