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首页> 外文期刊>European journal of organic chemistry >Synthesis of amino- and bis(bromomethyl)-substitued bi- and tetradentate N-heteroaromatic ligands: Building blocks for pyrazino-functionalized fullerene dyads
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Synthesis of amino- and bis(bromomethyl)-substitued bi- and tetradentate N-heteroaromatic ligands: Building blocks for pyrazino-functionalized fullerene dyads

机译:氨基和双(溴甲基)取代的双齿和四齿N-杂芳族配体的合成:吡嗪基官能化富勒烯二元组的结构单元

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In this paper we describe the synthesis of amino- and bis(bromomethyl)-substituted derivatives of phenanthroline (phen), pyrazino[2,3-f]-phenanthroline (pphen), dipyrido[3,2-a:2',3'c]phenazine (dppz), pyrazino[2,3-i]dipyrido[3,2-a:2',3'c]phenazine, 2,3-bis(2-pyridyl)pyrazine (dpq), 2,3-bis(2-pyridyl)quinoxaline (dpq) and 7,8-bis(2-pyridyl)pyrazino[2,3g]quinoxaline. These substituted bi- and tetradentate N-heteroaromatic ligands are potential synthons for the preparation of the fullerene ligands 4-9. The diketones, 1,10-phenanthroline-5,6-dione 11a (phendione), 2,2-pyridyl 11b and 1,4-dibromo-2,3-butanedione 33 were used as starting materials. Phendione was converted into the phendiamine 13 by a two-step synthesis via the dioxime of the diketone 11a. Amino-substituted dppz and dpq derivatives were obtained by the reduction of the corresponding nitro compounds that were obtained by the Schiff base condensation of the diketones 11a and 11b and the appropriate o-phenylenediamine derivatives. An alternative synthetic route to the diamines 20a and 20b by etosylation of the diamino -substituted dppz and dpq ligands is also presented. Synthesis of the bis(bromomethyl) -substituted pphen, dpp, dppz and dpq derivatives was performed by the photochemical addition of bromine. Alternatively, synthesis of the his (bromomethyl) -substituted pphen, pdppz and pdpq is also possible by the condensation of 1,4-dibromo-2,3-butanedione 33 and phendiamine or the diamino-substituted dppz and dpq derivatives. The latter two compounds can be also prepared by the condensation of diketones 11a and 11b with 6,7-diamino-2,3-bis(bromomethyl)quinoxaline. Although the synthesis of some dppz and dpq ligands is already published, we herein present improved or alternative synthetic strategies leading to higher yields and/or higher purity of these N-heteroaromatic ligands. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.
机译:在本文中,我们描述了菲咯啉(phen),吡嗪并[2,3-f]-菲咯啉(pphen),双吡啶[3,2-a:2',3]的氨基和双(溴甲基)取代衍生物的合成'c]吩嗪(dppz),吡嗪并[2,3-i] dipyrido [3,2-a:2',3'c]吩嗪,2,3-双(2-吡啶基)吡嗪(dpq),2 3-双(2-吡啶基)喹喔啉(dpq)和7,8-双(2-吡啶基)吡嗪并[2,3g]喹喔啉。这些取代的双齿和四齿N-杂芳族配体是用于制备富勒烯配体4-9的潜在合成子。二酮,1,10-菲咯啉-5,6-二酮11a(苯二酮),2,2-吡啶基11b和1,4-二溴-2,3-丁二酮33用作起始原料。经由二酮11a的二肟通过两步合成将苯二甲酮转化为苯二胺13。通过还原相应的硝基化合物获得氨基取代的dppz和dpq衍生物,该硝基化合物是通过二酮11a和11b与适当的邻苯二胺衍生物的席夫碱缩合反应而获得的。还提出了通过二氨基取代的dppz和dpq配体的烷基化来生成二胺20a和20b的替代合成途径。双(溴甲基)取代的pphen,dpp,dppz和dpq衍生物的合成通过光化学添加溴来进行。或者,通过1,4-二溴-2,3-丁二酮33与苯二胺或二氨基取代的dppz和dpq衍生物的缩合,也可以合成组氨酸(溴甲基)取代的pphen,pdppz和pdpq。后两种化合物也可以通过将二酮11a和11b与6,7-二氨基-2,3-双(溴甲基)喹喔啉缩合而制备。尽管一些dppz和dpq配体的合成方法已经发表,但我们在此提出了改进的或替代的合成策略,导致这些N-杂芳族配体的产率更高和/或纯度更高。 (c)Wiley-VCH Verlag GmbH&Co.KGaA,69451,德国魏因海姆,2006年。

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