146449-90-3Relevant articles and documents
CYCLOHEXADIENE FULLERENE DERIVATIVES
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Page/Page column 79; 80; 85; 86, (2015/03/28)
The invention relates to novel fullerene derivatives, to methods for their preparation and educts or intermediates used therein, to mixtures and formulations containing them, to the use of the fullerene derivatives, mixtures and formulations as organic semiconductors in, or for the preparation of, organic electronic (OE) devices, especially organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising, or being prepared from, these fullerene derivatives, mixtures or formulations.
Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions
Thiemann, Thies,Tanaka, Yasuko,Iniesta, Jesus,Varghese, H. Tresa,Pannicker, C. Yohannan
experimental part, p. 732 - 736 (2010/03/24)
Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.
Synthesis and Properties of Liquid Crystalline 4,4 -Dialkoxy-2'-Methyl-p-Terphenyls
Yu, Z. N.,Tu, H. L.,Wan, X. H.,Chen, X. F.,Zhou, Q. F.
, p. 41 - 56 (2007/10/03)
A new series of laterally substituted terphenyl compounds, 4,4 -dialkoxy-2'-methyl-p-terphenyls (n = 1-12), were synthesized. Their liquid crystallinities were characterized by means of polarizing optical microscopy (POM), differential scanning calorimetry (DSC), and X-ray difraction (XRD). The influence of the length of the terminal alkoxy groups on the liquid crystalline behavior was investigated. It was found that the compounds with shorter end chains (n a smectic A mesophase is exhibited for those with longer end chains (9 = n = 12).
