首页> 外文期刊>Bulletin of the Chemical Society of Japan >Facile Preparation of Highly Luminescent Materials by Electrostatic Immobilization of Anionic Metal Complex onto Anion-Exchanger as Exemplified with Tri-Terbium(III) Cluster Complex of Thiacalix[4]arene-p-tetrasulfonate
【24h】

Facile Preparation of Highly Luminescent Materials by Electrostatic Immobilization of Anionic Metal Complex onto Anion-Exchanger as Exemplified with Tri-Terbium(III) Cluster Complex of Thiacalix[4]arene-p-tetrasulfonate

机译:通过抗神经金属络合物在阴离子交换器上的静电固化物的容纳制备,其与ThiCalix的三铽(III)簇复合物举例说明[4]芳烯-P-四硫磺酸盐

获取原文
获取原文并翻译 | 示例
       

摘要

We propose a strategy to prepare luminescence materials via simple and organic solvent-free fashion by mixing an anionic luminescent complex with an anion exchanging support. As a proof-of-concept, we employed the heptaanionic Tb-III complex Tb(3)TCAS(2) (TCAS = thiacalix[4]arene-p-tetrasulfonate) and QAE Sephadex A-25, a dextran support bearing anion exchanging groups. By stirring a mixture of TCAS and dextran (1.0 mu mol Tb(3)TCAS(2)/50 mg dextran), 99.8% of Tb(3)TCAS(2) was successfully immobilized within 2 h. The electrostatic interactions were strong enough to irreversibly bind Tb(3)TCAS(2) to the dextran. The material exhibited Tb-III-centered luminescence upon excitation of the TCAS center. The luminescent lifetime and quantum yield were 1.18 ms and 45.5%, respectively. When the amount of Tb(3)TCAS(2) immobilized on the dextran was reduced to 1.0 nmol/50 mg dextran, the lifetime increased to 1.32 ms, suggesting concentration quenching above 1.0 mu mol Tb(3)TCAS(2)/50 mg dextran. On the other hand, the luminescence quantum yield decreased to 3.1%, suggesting that the absorption of excited light by the support was not negligible. Preparation of the materials in D2O resulted in increases in the lifetime and quantum yields to 1.32 ms and 44%, respectively.
机译:我们提出了一种通过将阴离子发光络合物与阴离子交换载体混合来制备发光材料的策略来制备发光材料。作为概念验证,我们使用庚酮Tb-III复合TB(3)TCAS(2)(TCAS = ThiCalix [4]芳烯-P-四硫酸盐)和QAE Sephadex A-25,葡聚糖支撑轴承阴离子交换团体。通过搅拌TCAs和葡聚糖的混合物(1.0μmolTb(3)TCAs(2)/ 50mg葡聚糖),99.8%的TB(3)TCAs(2)在2小时内成功地固定。静电相互作用足以不可逆地将Tb(3)TCAs(2)结合到葡聚糖中。该材料在TCAS中心的激发时表现出CTB-III的发光。发光寿命和量子产率分别为1.18毫秒和45.5%。当固定在葡聚糖上的TB(3)TCAS(2)的量降低至1.0nmol / 50mg葡聚糖时,寿命增加至1.32ms,表明浓度猝灭以上1.0μmolTB(3)TCAS(2)/ 50 Mg德克兰。另一方面,发光量子产率降至3.1%,表明通过载体吸收激发光并不可忽略不可忽略。 D2O中材料的制备导致寿命和量子的增加,分别为1.32ms和44%。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号