620180-53-2Relevant articles and documents
Containing azo phenyl the xylosides and its preparation method and application
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Paragraph 01345-0136, (2017/05/02)
The invention belongs to the field of catalytic reaction engineering, and particularly relates to synthetic glucoside containing an azobenzene group, and application of the glucoside serving as an ultraviolet controlled-release material. The glucoside containing an azobenzene group has a structure as shown in Formula (I). The glucoside containing an azobenzene group can be used for preparation of ultraviolet sensitive liposome, and has favorable structural stability, biological targeting property, biocompatibility and in-vivo degradability.
Liquid-crystalline polymorphism of symmetrical azobananas: Bis(4-(4-alkylphenyl)azophenyl) 2-nitroisophtalates
Zygadlo,Dardas,Nowicka,Hofmann,Galewski
, p. 283 - 291 (2011/08/02)
In this paper we present a series of novel compounds, bis(4-(4-alkylphenyl) azophenyl) 2-nitroisophtalates, which exhibit nematic and banana-type liquidcrystalline phases. The alkyl chain length varies from 1 to 18 carbons. The first ten members of this series exhibit nematic phase. The last eleven compounds exhibit banana-type liquid crystalline phases. The propyl and pentyl derivatives have extra second type of banana mesophase. Copyright Taylor & Francis Group, LLC.
Photo-induced molecular-recognition-mediated adhesion of giant vesicles
Mansfeld, Friederike M.,Feng, Guoqiang,Otto, Sijbren
experimental part, p. 4289 - 4295 (2009/12/06)
Few methods currently exist for controlling vesicle-vesicle adhesion. We now report a new system, based upon a multivalent guest and an amphiphilic receptor with a photo-isomerisable anchor that can be incorporated into lipid vesicles of different sizes.
A convenient synthesis of novel mercapto-ended azobenzene derivatives
Haiying, Li,Zhongfan, Liu
, p. 3779 - 3785 (2007/10/03)
Treatment of the product from the Diazo-Coupling reaction of p- alkylaniline with 1,3-dibromopropane in THF affords intermediate compounds n- C(n)H(2n+1)AzoO(CH2)(m)Br. Subsequent treatment of these intermediate with thiourea in ethanol at refl