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对具有各种发光特性的铽或铕核树枝状大分子配合物的X射线吸收精细结构研究。

XAFS studies of Tb or Eu cored dendrimer complexes with various properties of luminescence.

作者信息

Seto T, Kawa M, Sugiyama K, Nomura M

机构信息

Yokohama Laboratory, Centre for Analytical Chemistry and Science (CACs), Inc., Japan.

出版信息

J Synchrotron Radiat. 2001 Mar 1;8(Pt 2):710-2. doi: 10.1107/s0909049500015910.

Abstract

We studied the extended X-ray absorption fine structure (EXAFS) of Tb or Eu L3-edge of Tb(III) or Eu(III)-cored complexes of different luminescence to which different poly(benzyl ether) dendrons coordinated. The complexes were prepared via a ligand exchange reaction of dendritic carboxylic acid and acetate. Results show that (a) the Eu complex of the first generation of the 3,4- or 3,5-dibenzyloxyphenyl type had a coordination structure different from that of the 2,4-dibenzyloxyphenyl type; (b) the Eu complex of the first generation of 3,5-dinaphthylmethoxyphenyl type had a Eu-O coordination number higher than the total number of oxygen atoms in the carboxylate groups; (c) the Tb complex of the bulky fourth generation had a Th-O coordination number higher than that of the first generation. These results show that the different poly(benzyl ether) dendrons cause the different coordination, which might differently influence the luminescence properties of the complexes.

摘要

我们研究了不同发光的、与不同聚(苄基醚)树枝状分子配位的Tb(III)或Eu(III)核配合物的Tb或Eu L3边扩展X射线吸收精细结构(EXAFS)。这些配合物通过树枝状羧酸与乙酸盐的配体交换反应制备。结果表明:(a)第一代3,4-或3,5-二苄氧基苯基型的Eu配合物具有与2,4-二苄氧基苯基型不同的配位结构;(b)第一代3,5-二萘基甲氧基苯基型的Eu配合物的Eu-O配位数高于羧基中氧原子的总数;(c)庞大的第四代Tb配合物的Th-O配位数高于第一代。这些结果表明,不同的聚(苄基醚)树枝状分子导致不同的配位,这可能会对配合物的发光性质产生不同的影响。

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