检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:谢光勇[1] 曾艺 罗德荣 尤庆亮[2] 罗亚妮 杨子锋 XIE Guangyong;ZENG Yi;LUO Derong;YOU Qingliang;LUO Yani;YANG Zifeng(Hubei Provincial Key Laboratory of Catalysis and Materials Science,College of Chemistry and Materials Science,South-Central University for Nationalities,Wuhan 430074,China;Key Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of Education,School of Chemical and Environmental Engineering,Jianghan University,Wuhan 430056,China)
机构地区:[1]中南民族大学化学与材料科学学院,催化材料科学湖北省重点实验室,武汉430074 [2]江汉大学化学与环境工程学院,光电化学材料与器件教育部重点实验室,武汉430056
出 处:《中南民族大学学报(自然科学版)》2019年第3期327-330,共4页Journal of South-Central University for Nationalities:Natural Science Edition
基 金:国家自然科学基金资助项目(21172269);湖北省教育厅科学研究计划(B2017270)
摘 要:以2,2′-二羟基联苯为原料,经过羟基保护、羟基邻位甲酰化、去保护等反应,合成了2,2′-二羟基-[1,1′-联苯基]-3,3′-二醛,再与2-丙硫基苯胺通过希夫碱反应合成了一种新型的双水杨醛亚胺配体3,3′-双-[(2-丙硫基)-苯亚胺]-2,2′-二羟基联苯(5).所合成的化合物通过核磁氢谱、元素分析、红外光谱等手段进行了表征,目标产物5通过X射线单晶衍射进一步证实了其结构.双水杨醛亚胺配体5晶体结构表明两个相连的苯环不共平面,二面角为63.14°,且两个水杨醛亚胺中配位原子所在的键长、键角不同,说明与中心金属配位时产生了两个不同的活性中心.2,2′-dihydroxy-[1,1′-biphenyl]-3,3′-dicarbaldehyde was synthesized by hydroxyl protection,ortho formylation and deprotection reactions with 2,2′-dihydroxybiphenyl as starting material,followed by reaction with 2-propylthio aniline to obtain a new biphenol diimine ligand named 3,3′-bis-[(2-propylthio)-phenylimino]-2,2′-dihydroxybiphenyl(5).All the compounds were characterized by^1H NMR,FTIR,and elemental analysis.The ligand 5 was further characterized by X-ray single crystal diffraction,which indicated that the two linked phenyl rings were not coplanar,with a dihedral angle of 63.14°.The bond lengths and bond angles around the coordination atoms on two salicylaldimine were also different,suggesting that two different active centers may exist when coordinated with metals.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.3