A New Fluoride Luminescence Quencher Based on a Nanostructured Covalently Bonded Terbium Hybrid Material

2010 ◽  
Vol 114 (32) ◽  
pp. 13879-13883 ◽  
Author(s):  
Qianming Wang ◽  
Chaoliang Tan ◽  
Hongyu Chen ◽  
Hitoshi Tamiaki
2005 ◽  
Vol 109 (44) ◽  
pp. 20854-20857 ◽  
Author(s):  
Wenfang Sun ◽  
Qiu Dai ◽  
James G. Worden ◽  
Qun Huo

2005 ◽  
Vol 20 (3) ◽  
pp. 592-598 ◽  
Author(s):  
Qianming Wang ◽  
Bing Yan

The syntheses of modified ortho or meta methylbenzoic acid by (3-aminopropyl)triethoxysilane and the preparation of their corresponding organic–inorganic molecular-based hybrid material with the two components equipped with covalent bonds are described. The organic part is a derivative of methyl benzoic acid, which is used to coordinate to Tb3+ and further introduced into silica matrices by Si–O bonds after hydrolysis and polycondensation processes. The Judd–Ofelt theory proves that covalency increases along with increasing reciprocal energy difference between the 4fN and 4fN−15d1 configurations. Ultraviolet absorption, phosphorescence spectra, and luminescence spectra were applied to characterize the photophysical properties of the obtained hybrid material, and the above spectroscopic data reveal that the triplet energy of modified methyl benzoic acid matches with the emissive energy level of Tb3+. In this way, the intramolecular energy transfer process took place within these molecular-based hybrids, and strong green emission of Tb3+ was obtained.


2015 ◽  
Vol 33 (9) ◽  
pp. 905-910
Author(s):  
Xudong YU ◽  
Jingyin LI ◽  
Yajuan LI ◽  
Lijun GENG ◽  
Xiaoli ZHEN ◽  
...  

2016 ◽  
Vol 227 ◽  
pp. 660-667 ◽  
Author(s):  
Yajuan Li ◽  
Dongyan Xie ◽  
Xuelei Pang ◽  
Xudong Yu ◽  
Tao Yu ◽  
...  

Author(s):  
Richard J. Spontak ◽  
Steven D. Smith ◽  
Arman Ashraf

Block copolymers are composed of sequences of dissimilar chemical moieties covalently bonded together. If the block lengths of each component are sufficiently long and the blocks are thermodynamically incompatible, these materials are capable of undergoing microphase separation, a weak first-order phase transition which results in the formation of an ordered microstructural network. Most efforts designed to elucidate the phase and configurational behavior in these copolymers have focused on the simple AB and ABA designs. Few studies have thus far targeted the perfectly-alternating multiblock (AB)n architecture. In this work, two series of neat (AB)n copolymers have been synthesized from styrene and isoprene monomers at a composition of 50 wt% polystyrene (PS). In Set I, the total molecular weight is held constant while the number of AB block pairs (n) is increased from one to four (which results in shorter blocks). Set II consists of materials in which the block lengths are held constant and n is varied again from one to four (which results in longer chains). Transmission electron microscopy (TEM) has been employed here to investigate the morphologies and phase behavior of these materials and their blends.


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