14163-03-2Relevant articles and documents
Recyclable Transition Metal Catalysis using Bipyridine-Functionalized SBA-15 by Co-condensation of Methallylsilane with TEOS
Han, Ye Ri,Kim, Jae Soon,Park, Woo-Jin,Lee, Chang-Hee,Cheon, Jinwoo,Jun, Chul-Ho
supporting information, p. 197 - 201 (2021/01/18)
Well-defined recyclable Pd- and Rh-bipyridyl group-impregnated SBA-15 catalysts were prepared for C?C bond coupling reaction and selective hydrogenation reactions, respectively. These SBA-15 derived ligands for the catalysts were prepared by direct and indirect co-condensation method using bipyridyl-linked methallylsilane. This indirect method, involving methoxysilane generated from methallylsilane shows higher loading efficiency of transition metal catalysts on SBA-15 than the direct use of methallylsilane.
Synthesis and Screening of Modified 6,6′-Bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydrobenzo[e][1,2,4]triazin-3-yl)-2,2′-bipyridine Ligands for Actinide and Lanthanide Separation in Nuclear Waste Treatment
Afsar, Ashfaq,Distler, Petr,Harwood, Laurence M.,John, Jan,Westwood, James
, p. 10517 - 10520 (2016/11/17)
Effects of chloro and bromo substitution at the 4-position of the pyridine ring of 6,6′-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydrobenzo[e][1,2,4]triazin-3-yl)-2,2′-bipyridine (CyMe4-BTBP) have been studied with regard to the extraction of Am(III) from Eu(III) and Cm(III) from 0.1-3 M HNO3. Similarly to CyMe4-BTBP, a highly efficient (DAm > 10 at 3 M HNO3) and selective (SFAm/Eu > 100 at 3 M HNO3) extraction was observed for Cl-CyMe4-BTBP and Br-CyMe4-BTBP in 1-octanol but in the absence of a phase-transfer agent.
Synthesis of a novel dinuclear ruthenium polypyridine dye for dye-sensitized solar cells application
Zalas,Gierczyk,Klein,Siuzdak,P?dziński,?uczak
supporting information, p. 381 - 387 (2013/11/06)
A new dinuclear ruthenium(II) polypyridine complex has been successfully synthesized. The new compound has been characterized by spectroscopic and electrochemical methods. Its potential application as a sensitizing dye in dye-sensitized solar cells has been checked under AM 1.5 G irradiation conditions (100 mW cm-2) and its performance was compared to that of a commercially available mononuclear analogous dye. The overall light-to-electricity conversion efficiency of the photovoltaic device sensitized by the new dinuclear dye has been found to be over 2.5 times lower than that sensitized by the commercial analogue, despite a much higher extinction coefficient of the former dye. The probable reasons for the lower photovoltaic activity are discussed.