Tetrathiafulvalenyl-acetylacetonate complexes of difluoroboron
摘要:
A series of tetrathiafulvalene (TTF) derivatives functionalized by one or two beta-diketonatoboron difluoride groups were synthesized through the addition of borontrifluoride to TTF Substituted by one or two acetylacetone functions. The influence of the beta-diketonatoboron difluoride moiety on the redox properties of the TTF has been investigated by cyclic voltammetry. (C) 2009 Elsevier Ltd. All rights reserved.
A Multi-Redox Responsive Cyanometalate-Based Metallogel
作者:Kiyotaka Mitsumoto、Jamie M. Cameron、Rong-Jia Wei、Hiroyuki Nishikawa、Takuya Shiga、Masayuki Nihei、Graham N. Newton、Hiroki Oshio
DOI:10.1002/chem.201605542
日期:2017.1.31
A TTF‐based (TTF=tetrathiafulvalene) tridentate ligand (α‐(4′‐methyl‐4,5‐di‐n‐dodecylthylthiotetrathiafulvalene‐5′‐ylthio)‐ α′‐[2,2,2‐tris(1‐pyrazolyl)ethoxy]‐p‐xylene) (L) with long‐chain alkyl moieties was prepared in order to obtain a new multi‐redox active gelator based on a mixed‐metal octanuclear complex [FeIII4NiII4(CN)12(tp)4(L)4](BF4)4 (1). The magnetism, electrochemistry, and gelation behavior
基于TTF的(TTF = tetrathiafulvalene)三齿配体(α-(4'-甲基-4,5-二-n-十二烷基硫基四硫富瓦烯-5'-基硫基)-α ′-[2,2,2-三三(1-制备具有长链烷基部分的吡唑基[乙氧基]-乙氧基]-对二甲苯](L),以便获得基于混合金属八核络合物[Fe III 4 Ni II 4(CN)12的新型多氧化还原活性胶凝剂。(tp)4(L)4 ](BF 4)4(1)。磁,电化学,和凝胶化的行为1进行了研究和1,2-二氯苯中的溶液1所显示的在室温下显示出热可逆的胶凝行为。此外,显示1的凝胶相经历了室温的凝胶转化为溶胶的转变,这是由F 4 TCNQ或[Fe II(Cp *)2 ]引起的胶凝剂复合物的氧化和还原分别诱导的。
New redox active ligands involving a tetrathiafulvalene vinylogue backbone
作者:Michel Guerro、Ngoc Ha Pham、Julien Massue、Nathalie Bellec、Dominique Lorcy
DOI:10.1016/j.tet.2008.03.032
日期:2008.5
Two synthetic approaches towards a new bisthiopicoline substituted vinylogous tetrathiafulvalene (TTFV) are described. As evidenced by electrochemistry and 1H NMR studies, this redoxactiveligand shows excellent coordinating properties towards Zn2+ metal ion.
描述了一种针对新的双硫代吡啶啉取代的乙烯基四硫富富瓦烯(TTFV)的两种合成方法。如通过电化学和1 H NMR研究所证明的,该氧化还原活性配体对Zn 2+金属离子显示出优异的配位性能。
Tetrathiafulvalenyl-acetylacetonate complexes of difluoroboron
作者:Michel Guerro、Thierry Roisnel、Dominique Lorcy
DOI:10.1016/j.tet.2009.05.041
日期:2009.8
A series of tetrathiafulvalene (TTF) derivatives functionalized by one or two beta-diketonatoboron difluoride groups were synthesized through the addition of borontrifluoride to TTF Substituted by one or two acetylacetone functions. The influence of the beta-diketonatoboron difluoride moiety on the redox properties of the TTF has been investigated by cyclic voltammetry. (C) 2009 Elsevier Ltd. All rights reserved.