Synthesis, growth, spectral, thermal and photoluminescence properties of a new semiorganic NLO crystal—Thiosemicarbazide lithium chloride [TSLC]

Thiosemicarbazide lithium chloride [TSLC] a new semiorganic nonlinear optical crystal has been synthesized. Single crystals by TSLC have been grown by slow evaporation solution growth technique at room temperature. Chemical composition of the synthesized material was confirmed by elemental analysis. Powder X-ray diffraction (XRD) pattern of the grown crystal has been studied. Functional groups present in the materials were identified by FT IR spectral analysis ranging between 4000 and 450 cm⁻¹. The optical transmission was studied through UV-vis spectrophotometer. Thermal analysis is carried out on the crystal and inferred to be stable at 176 °C. The second harmonic generation (SHG) of the TSLC crystal was confirmed using Nd:YAG laser and also fluorescence spectral analysis is carried out for the TSLC crystal.     

发红色荧光铽配合物的合成及荧光性能的研究

以二苯甲酰甲烷(HDBM)为第一配体,邻菲罗啉(phen)和二吡啶并[3,2-a:2',3'-c]哇喔啉(dpq)为第二配体合成两种三元铽配合物,并进行元素分析、稀土络合滴定、摩尔电导率、红外光谱、紫外光谱、荧光激发和发射光谱的测定,推测化合物的组成分别为:Tb(DBM)3phen,Tb(DBM)3dpq.DBM通过氧...     

铽－甲基吲哚乙酰丙酮三元配合物发光过程研究

测定和分析了ＲＥ．Ｌ１．Ｌ２（ＲＥ＝Ｔｂ（Ⅲ）、Ｇｄ（Ⅲ），Ｌ１＝３Ｍ（３甲基吲哚－１－乙酰基丙酮），Ｌ２＝ＴＰＰＯ、Ｐｈｅｎ、Ｄｉｐｙ）三元配合物的荧光光谱、磷光光谱、磷光寿命及变温荧光光谱等．讨论了Ｔｂ（Ⅲ）与配体之间的能级匹配和Ｌ１与Ｌ２的三重态之间传能的问题，说明了影响这些三元配合物荧光效率的主要因素及其发光过程．     

Luminescent molecular hybrid system derived from 2-furancarboxylic acid and silylated monomer coordinated to rare earth ions

In this study, silica-based organic-inorganic hybrids were prepared by the sol-gel method. Tetraethoxysilane (abbreviated as TEOS) and a kind of monomer (abbreviated as FA-APES) derived from modified 2-furancarboxylic acid (abbreviated as FA) with (3-aminopropyl)triethoxysilane (abbreviated as APES) were used as the inorganic and organic fragments, respectively. Coordination reaction between lanthanides (europium and terbium ions) and CO group of the monomer happened simultaneously. And after days of aging process the resultant materials showed characteristic luminescence of lanthanides. The enhancement of luminescence can be seen by the comparison with simply doped lanthanide hybrid systems. And it can be explained by the coordination ability of the organic counterpart. IR, NMR, UV-vis absorption, low-temperature phosphorescence spectroscopy and fluorescence spectroscopy were applied to characterize and the above spectroscopic data revealed that the triplet state energy of organic ligand matches with the emissive energy level of lanthanides (especially of Tb³⁺).     

Transition from rigid to flexible structures in micelles of Undecylammonium chloride in aqueous solutions of NaCl

Small angle neutron scattering (SANS) data for Undecylammonium chloride (UAC) in heavy water in the presence of NaCl 0.0428 and 0.3422 M are consistent with the presence of elongated micelles. This micellar shape has been adopted to analyze viscosity data of UAC in water in the presence of NaCl. The results obtained from this last technique are consistent with the increase of the micelle aggregation number with increasing the surfactant concentration. Micelles change from prolate ellipsoidal shape to cylindrical and wormlike shapes by increasing the added NaCl concentration and surfactant concentrations. The differences between results for the micelle aggregation number calculated from viscosity, SANS and light scattering data have been attributed to the solvent effect on micelle formation as well as changes in the size, shape and flexibility of the micelle. Viscosity data provide qualitative information on the effect of the added NaCl concentration and surfactant concentration on the size, shape, flexibility of the micelles in diluted solutions.     

Effect of the End Groups and the Solvent on the Gelation of the Hybrid Materials from Poly (Vinyl Chloride) (PVC) and Oligo Phenylene Vinylene (OPV)

Abstract

The role of the end-groups of three oligophenylene vinylene (OPV) and the solvents on the hybrid materials from poly (vinyl chloride) (PVC) and the OPV are examined. The gelation of the three organogel OPVs and of the hybrid materials in bromobenzene and benzyl alcohol was characterized. The morphology, as well as the thermodynamic properties, of these OPV and hybrid materials showed that they depended mostly on the solvent and very little on the different end-groups located on the OPV backbones.     

A Highly Stable (4, 8)-Connected Tb-MOF Exhibiting Efficiently Luminescent Sensing towards Nitroimidazole Antibiotics

A robust 4,8-connected Tb-based metal-organic framework (Tb-MOF) with paddle wheel-shaped {Tb₂(COO)₄} subunits extended by C₃-symmetric 3,3',3''-[1,3,5-benzenetriyltris(carbonylimino)]tris-benzoate connector was hydrothermally synthesized, showing highly environmental stability, good dispersion and intense green emission in water system. Resulting critically from the well suppressed absorption towards the excitation energy, the Tb-MOF exhibits rapid and efficient fluorescent response towards nitroimidazole antibiotics with strong quenching constants and low detection limits of 1.59 × 10⁴ m ^–1 and 2.4 μM for metronidazole as well as 1.62 × 10⁴ m ^–1 and 2.9 μM for dimetridazole. Moreover, the sensitive and selective identification of the Tb-MOF has strong anti-interference and excellent regeneration ability, which endows the promising applications of the Tb-MOF as fluorescent sensing materials.     

Visible-Light-Induced Vicinal Dichlorination of Alkenes through LMCT Excitation of CuCl2

This work demonstrates photoredox vicinal dichlorination of alkenes, based on the homolysis of CuCl₂ in response to irradiation with visible light. This catalysis proceeds via a ligand to metal charge transfer process and provides an exciting opportunity for the synthesis of 1,2-dichloride compounds using an inexpensive, low-molecular-weight chlorine source. This new process exhibits a wide substrate scope, excellent functional group tolerance, extraordinarily mild conditions and does not require external ligands. Mechanistic studies show that the ready formation of chlorine atom radicals is responsible for the facile formation of C−Cl bonds in this synthetic process.     

超声雾化液体除湿系统对室内空气品质的影响

研究了超声雾化液体除湿空调系统对室内空气品质的影响,得到室内空气中氯化锂质量浓度的安全阈值为70μg/m~3.通过实验分析了入口溶液中氯化锂的质量分数(w_i)、除雾器孔隙率等对空气带液量的影响.当w_i由31.5%上升至38.8%时,空气带液量也随之上升,最高为26.93μg/m~3.除雾器的孔隙率显著影响空气带液量,应使用孔隙率低于93.5%的丝网除雾器.在最不利工况下,该系统空气带液量未超过安全阈值,表明对室内空气品质没有影响.研究成果对超声雾化液体除湿系统的推广有一定指导意义.     

氯柱硼镁石在氯化镁水溶液中相转化平衡液相的红外光谱分析

采用差示FTIR光谱技术,研究了氯柱硼镁石在30℃下浓度为0.5,12和18％MgCl_2水溶液中溶解及相转化平衡饱和水溶液中硼氧配阴离子的FTIR光谱。给出了溶液中硼氧配阴离子的FTIR光谱振动频率的归属,515cm~(-1)为单和二硼氧配阴离子特征峰,630cm~(-1)为三硼氧配阴离子特征峰,550cm~(-1)为四硼氧配阴离子特征峰。对饱和水溶液中硼氧配阴离子的存在形式及其相互作用以及与相转化析出固相的关系进行了讨论。