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《材料导报》期刊社  2017, Vol. 31 Issue (8): 11-16    https://doi.org/10.11896/j.issn.1005-023X.2017.08.003
  材料研究 |
两种冠醚环化二硫纶配体的Ni配合物的合成、结构及光电性质研究*
张睿1, 顾晓龙1, 庞欢2
1 扬州市职业大学生物与化工工程学院, 扬州 225009;
2 扬州大学化学化工学院, 扬州 225002
Synthesis, Structure and Photoelectric Properties of Two Novel Nickel(Ⅱ) Complexes Containing Crown Ether Annelated Dithiolate Ligand
ZHANG Rui1, GU Xiaolong1, PANG Huan2
1 School of Biological and Chemical Engineering,Yangzhou Polytechnic College, Yangzhou 225009;
2 College of Chemistry and Chemical Engineering,Yangzhou University, Yangzhou 225002
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摘要 以配体Ia、Ib和Ni(dbbpy)Cl2(dbbpy=4,4′-二-叔丁基-2,2′-联吡啶)反应,合成了两种新型冠醚环化二硫纶配体的Ni(Ⅱ)配合物1和2。经1H NMR、IR、MS和元素分析表征了二者的结构,并解析了其晶体结构,初步测定了其光电响应性质。结果表明,配合物2对Li+有较明显的响应,ΔE1/21=35 mV(30倍Li+),对碱金属离子Na+和K+均无明显响应。同时配合物1和2在室温下均有明显的溶剂变色现象。
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张睿
顾晓龙
庞欢
关键词:  二硫纶镍(Ⅱ)配合物  冠醚衍生物  合成  单晶衍射  光电性能    
Abstract: Two novel nickel (Ⅱ) complexes(1 and 2) containing crown ether annelated dithiolate ligand were synthesized by reactions of Ia,Ib with Ni(dbbpy)Cl2(dbbpy=4,4′- di-tert-butyl-2,2′-bipyridine). The complexes′ structure were characterized by 1H NMR, IR, MS and elemental analysis. X-ray crystallography and photoelectric properties of these two compounds were also investigated.Complex 2 exhibited a significant response for Li+ ions with a large positive shift of ca. 35 mV. Moreover, both complexes (1 and 2) displayed solvatochromic behaviors.
Key words:  nickel(Ⅱ) complex containing dithiolate ligand    crown ether annelated derivative    synthesis    crystallography    photoelectric property
出版日期:  2017-04-25      发布日期:  2018-05-02
ZTFLH:  O61  
基金资助: 国家自然科学基金(21671170)
通讯作者:  庞欢:男,博士,教授,主要从事无机纳米化学研究 E-mail:panghuan@yzu.edu.cn   
作者简介:  张睿:女,1979年生,硕士研究生,主要从事无机化学研究 E-mail:z.tulip@163.com
引用本文:    
张睿, 顾晓龙, 庞欢. 两种冠醚环化二硫纶配体的Ni配合物的合成、结构及光电性质研究*[J]. 《材料导报》期刊社, 2017, 31(8): 11-16.
ZHANG Rui, GU Xiaolong, PANG Huan. Synthesis, Structure and Photoelectric Properties of Two Novel Nickel(Ⅱ) Complexes Containing Crown Ether Annelated Dithiolate Ligand. Materials Reports, 2017, 31(8): 11-16.
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https://www.mater-rep.com/CN/10.11896/j.issn.1005-023X.2017.08.003  或          https://www.mater-rep.com/CN/Y2017/V31/I8/11
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