26910-11-2Relevant academic research and scientific papers
N-(2-Alkoxyphenyl)-substituted double rhodanine indoline dyes for zinc oxide dye-sensitized solar cell
Matsui, Masaki,Shiota, Takahiro,Kubota, Yasuhiro,Funabiki, Kazumasa,Jin, Jiye,Yoshida, Tsukasa,Higashijima, Shinji,Miura, Hidetoshi
experimental part, p. 4286 - 4291 (2012/07/14)
The effect of N-(2-alkoxyphenyl) group in double rhodanine indoline dye on the performance of zinc oxide dye-sensitized solar cell was examined. Both Jsc and Voc were improved by introducing long alkoxy group due to prevention of H-a
Chemical synthesis, biological evaluation and structure-activity relationship analysis of azaisoindolinones, a novel class of direct enoyl-ACP reductase inhibitors as potential antimycobacterial agents
Deraeve, Céline,Dorobantu, Ioana Miruna,Rebbah, Farah,Le Quéméner, Frédéric,Constant, Patricia,Quémard, Anna?k,Bernardes-Génisson, Vania,Bernadou, Jean,Pratviel, Geneviève
supporting information; experimental part, p. 6225 - 6232 (2011/12/14)
The synthesis and biological evaluation of azaisoindolinone compounds embedding a lipophilic chain on the framework were performed. These compounds were designed as InhA inhibitors and as anti-Mycobacterium tuberculosis agents. Structure-activity relation
Monohalogenation of alkyl phenyl ethers in micellar and vesicular media
Jaeger, David A.,Clennan, Malgorzata Wegrzyn,Jamrozik, Janusz
, p. 1171 - 1176 (2007/10/02)
The rates and regioselectivities of monohalogenation of C6H5OR (1: a, R = C5H11;b, R = C9H19; c, R = C12H25) by chlorine water and bromine water to give 4-XC6/su
Synthesis and Liquid Crystalline Properties of 1-(trans-4-Alkylcyclohexylethyl)-4-Alkyl- and -4-Alkoxy-Benzenes, Their Ketone Precursors, and Some Lateral Fluoro-Derivatives
Gray, George W.,Lacey, David,Scrowston, Richard M.,Shenouda, Ibrahim G.,Toyne, Kenneth J.
, p. 101 - 116 (2007/10/02)
The preparation of some 1-(trans-4-alkylcyclohexylethyl)-4-alkyl- and -4-alkoxy-benzenes, their methylenecarbonyl linked analogues and their laterally fluoro- and bromo-substituted derivatives is reported.Twenty-four inter-related compounds have been prepared and the trends in their transition temperatures are discussed.Both the melting points and clearing points for these compounds are relatively low and, in general, SB and SA phases predominate.The suitability of these compounds as additives to SC materials has been assessed using two SC hosts.Keywords: Mesogenic cyclohexylethanes, mesogenic ketones, fuoro-substitution of mesogens
