Lanthanide induced formation of novel luminescent alginate hydrogels and detection features

被引:38
作者
Ma, Qianmin [2 ]
Wang, Qianming [1 ,2 ,3 ]
机构
[1] S China Normal Univ, Sch Chem & Environm, Minist Educ, Key Lab Theoret Chem Environm, Guangzhou 510006, Guangdong, Peoples R China
[2] S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
[3] Guangzhou Key Lab Mat Energy Convers & Storage, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogel beads; Alginate; Lanthanides; Dipicolinate; METALLO-SUPRAMOLECULAR GELS; RHEOLOGICAL BEHAVIOR; GELATION; RELEASE; COMPLEXES; BEADS; IONS;
D O I
10.1016/j.carbpol.2015.07.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Responsive photo-luminescent soft matters have led to the design of optical sensors and switches. In this research, two new organic-inorganic type hybrid hydrogels have been fabricated by the self-assembly of sodium alginate and lanthanide elements. The incorporation of europium ions (Eu3+) (or terbium ions (Tb3+)) was required for the gelation of the dissolved alginate and thermally stable gels were formed. It has been found that red/green emissions derived from lanthanide ions were clearly identified in pure aqueous media through the metal coordination interactions with assembled alginate. These supramolecular structures could partially prevent the Eu3+ (or Tb3+) from being attacked by high frequency vibrations. More importantly, the lanthanide luminescence could be switched "off-on" in the presence of the anthrax biomarker sodium dipicolinate (NaDPA). The detection limits (for NaDPA) were determined to be 8.3 x 10(-8) M and 9.0 x 10(-8) M based on Eu(III) and Tb(III) gel, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 23
页数:5
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