陕西师范大学学报(自然科学版)
陝西師範大學學報(自然科學版)
협서사범대학학보(자연과학판)
JOURNAL OF SHAANXI NORMAL UNIVERSITY(NATURAL SCIENCE EDITION)
2014年
6期
50-53,59
,共5页
偶辉%刘课艳%董雪芬%王彭敏%石先莹
偶輝%劉課豔%董雪芬%王彭敏%石先瑩
우휘%류과염%동설분%왕팽민%석선형
咔唑衍生物%乌尔曼偶联反应%树枝状分子
咔唑衍生物%烏爾曼偶聯反應%樹枝狀分子
잡서연생물%오이만우련반응%수지상분자
carbazole derivatives%Ullmann coupling reaction%dendrimer
以1,4-二溴苯和1,8-二碘联苯为原料分别与咔唑发生乌尔曼偶联反应制得两种相应的成对偶联分子,用 NBS 作为溴化试剂与这两种分子反应制得新型的多溴代产物:3,3′,6-三溴-1,4-双咔唑基苯、3,3′,6,6′-四溴-1,4-双咔唑基苯和3,3′,6-三溴-1,8-双咔唑基联苯。该溴化物与咔唑在铜催化下发生乌尔曼偶联反应制得3种新颖的树枝状咔唑类衍生物:3,3′,6-三(N-咔唑基)-1,4-双咔唑基苯、3,3′,6,6’-四(N-咔唑基)-1,4-双咔唑基苯、3,3′,6-三(N-咔唑基)-1,8-双咔唑基联苯。通过核磁、质谱分别对所合成的化合物进行了表征。
以1,4-二溴苯和1,8-二碘聯苯為原料分彆與咔唑髮生烏爾曼偶聯反應製得兩種相應的成對偶聯分子,用 NBS 作為溴化試劑與這兩種分子反應製得新型的多溴代產物:3,3′,6-三溴-1,4-雙咔唑基苯、3,3′,6,6′-四溴-1,4-雙咔唑基苯和3,3′,6-三溴-1,8-雙咔唑基聯苯。該溴化物與咔唑在銅催化下髮生烏爾曼偶聯反應製得3種新穎的樹枝狀咔唑類衍生物:3,3′,6-三(N-咔唑基)-1,4-雙咔唑基苯、3,3′,6,6’-四(N-咔唑基)-1,4-雙咔唑基苯、3,3′,6-三(N-咔唑基)-1,8-雙咔唑基聯苯。通過覈磁、質譜分彆對所閤成的化閤物進行瞭錶徵。
이1,4-이추분화1,8-이전련분위원료분별여잡서발생오이만우련반응제득량충상응적성대우련분자,용 NBS 작위추화시제여저량충분자반응제득신형적다추대산물:3,3′,6-삼추-1,4-쌍잡서기분、3,3′,6,6′-사추-1,4-쌍잡서기분화3,3′,6-삼추-1,8-쌍잡서기련분。해추화물여잡서재동최화하발생오이만우련반응제득3충신영적수지상잡서류연생물:3,3′,6-삼(N-잡서기)-1,4-쌍잡서기분、3,3′,6,6’-사(N-잡서기)-1,4-쌍잡서기분、3,3′,6-삼(N-잡서기)-1,8-쌍잡서기련분。통과핵자、질보분별대소합성적화합물진행료표정。
Three kinds of novel dendritic carbazole derivatives were designed and synthesized via three steps using 1,8-diiodobiphenyl and 1,4-dibromobenzene as starting material.In this process,two pairs of conjugate molecules,which were obtained through Ullmann coupling reaction between phenyldihalide and carbazole,reacted with NBS to generate three multi-brominated intermediates:3,3′,6-tribromo-1, 4-bis-carbazolyl-benzene,3,3′,6,6′-tetrabromo-1,4-bis-carbazolyl-benzene,3,3′,6- tribromo-1,4-bis-carbazolyl-biphenyl.Then,the desired novel dendritic carbazole derivatives including 3,3′,6-Tri(N-car-bazolyl)-1,4-bis-carbazolyl-benzene,3,3′,6,6′-Tetra (N-carbaolyl)-1,4-bis-carbazolybenzene,3,3′,6-Tri(N-carbazolyl)-1,8-bis-carbazolyl-biphenyl were formed through Ullmann coupling again with multi-brominated compounds and carbazole.The intermediates and target products were characterized by 1 H NMR,13 C NMR and MS.