Metal ion and anion coordination in the thiamine-[Pt-II(NO2)(4)](2-) system. Structures of a metal complex, Pt(thiamine)(NO2)(3), and two salts, (H-thiamine)[Pt(NO2)(4)]center dot 2H(2)O and (thiamine monophosphate)(2)[Pt(NO2)(4)]center dot 2H(2)O

Reaction of thiamine or thiamine monophosphate (TMP) with K2Pt(NO2)(4) afforded a metal complex, Pt(thiamine)(NO2)(3) (1), and two salt-type compounds, (H-thiamine)[Pt(NO2)(4)]. 2H(2)O (2) and (TMP)(2)[Pt(NO2)(4)]. 2H(2)O (3), which were structurally characterized by X-ray diffraction. In 1, the square-planar Pt2+ ion is coordinated to the pyrimidine N(1'), a usual metal-binding site, and three NO2- groups. The thiamine molecule exists as a monovalent cation in 1 and a divalent cation in 2 while the TMP molecule is a monovalent cation in 3. In each compound, thiamine or TMP adopts the usual F conformation and forms two types of host-guest-like interactions with anions, which are of the bridging forms, C(2)-H . . . anion . . . pyrimidine-ring and N(4'1)-H(...)anion(...)thiazolium-ring. In 3, there is an additional anion-bridging interaction between the pyrimidine and thiazolium rings of TMP, being of the form C(6')-H . . . anion . . . thiazolium-ring. The salts 2 and 3 show similar hydrogen-bonded cyclic dimers of thiamine or TMP between which the anions are held. Results are compared with those of the other thiamine-platinum complexes. (C) 2001 Elsevier Science B.V. All rights reserved.

Selective crystallization of BaF2 under a compressed Langmuir monolayer of behenic acid

Selective crystallization of BaF2 crystals under a compressed Langmuir monolayer of behenic acid [CH3(CH2)(20)COOH] has been studied by using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and energy-dispersive X-ray analysis. It was found that, in the absence of a monolayer, three kinds of crystals (Ba2ClF3, BaClF, and BaF2) can be obtained by mixing BaCl2 with a NH4F solution. However, in the presence of the monolayer of behenic acid, only BaF2 crystals appear at the monolayer-subphase interface and crystals have a special crystal face (100). During this process of crystallization, the monolayer plays a very important role and acts as a template that can preferentially select a special crystal and a special crystal face. The above results can be explained in terms of a specific molecular interaction between ions and the headgroups of the monolayer and specific electrostatic, geometric, and stereochemical interactions at the organic-inorganic interface.

我国稀土化学的进展

建国以来我国稀土化学研究取得了重要进展。本文概述了我国 50年来 ,特别是近 2 0年来在稀土的固体化学、稀土的生物无机化学、稀土的萃取化学和稀土的配位化学领域取得的一些代表性成果

The change of Eu3+-surroundings in the system Al2O3-B2O3 containing Eu3+ ions

The change of Eu3+-surroundings with the Al/B ratio varying from 4.5 to 2 and Eu/(Al + B) = 0.02, was investigated through X-ray diffraction, infrared spectra, excitation and emission spectra, and phonon sideband. The results show coexistence of the crystal phase Al18B4O33 and the amorphous phase and Eu3+ ions of the samples with the Al/B ratio from 3 to 2 are incorporated into the amorphous phase. It was also found that electron-phonon coupling strength decreases with the Al/B ratio from 3 to 2, non-radiative decay rate decreases, resulting in an increase of the Eu3+-emission intensity. (C) 1999 Elsevier Science Ltd. All rights reserved.

Electroluminescent devices based on monohexadecyl phthalate terbium

Electroluminescent devices with PVK film doped with monohexadecyl phthalate terbium and PBD were fabricated. The device structure of glass substrate/ITO/PPV/PVK:Tb(MHP)(3):PBD/Alq(3)/Al was employed. The emissive layer was formed by a spin-casting technique. The EL cells exhibited characteristic emission of terbium ions with a maximum luminance of 74 cd/m(2) at 18 V. (C) 1998 Elsevier Science S.A. All rights reserved.

均相稀土催化苯乙烯均聚及其与异戊二烯共聚

采用新型稀土催化体系氯代三氟乙酸钕（Ｎｄ）－烷基铝（Ａｌ）－卤代烃（Ｘ），引发苯乙烯（Ｓｔ）均聚及其与异戊二烯（Ｉｐ）共聚。研究了催化体系各组分及陈化方式、Ｘ和Ａｌ种类及用量、溶剂种类等因素对苯乙烯聚合的影响，并用稀土催化剂实现了Ｓｔ－Ｉｐ嵌段共聚。用ＩＲ，ＮＭＲ及ＤＳＣ等方法表征了聚合物的结构，合成出的Ｓｔ－Ｉｐ二嵌段共聚物中，Ｉｐ链节以反式－１，４－结构为主，含少量３，４－结构，几乎不含顺式－１，４－结构。

LnSrNiO_(4-λ)系列复合氧化物的物化性质与对NO分解的催化性能

用柠檬酸络合法合成了Ｋ２ＮｉＦ４结构的ＬｎＳｒＮｉＯ４－λ（Ｌｎ＝Ｌａ，Ｐｒ，Ｎｄ，Ｓｍ，Ｇｄ）系列稀土取代类钙钛石型复合氧化物催化剂，对该系列催化剂的固态物理、化学性质及其对ＮＯ分解的催化性能进行研究。结果表明，该系列复合氧化物催化剂对ＮＯ分解活性都很高，在此基础上对该系列复合氧化物中稀土元素对ＮＯ分解反应的取代效应进行了探讨。

Luminescence and energy transfer phenomena of several rare earth ions in the CaAl2B2O7

The luminescence properties of Ce3+, Gd3+, and Tb3+ have been investigated in the compound CaAl2B2O7. The single excitation band peaking at about 320 nm and single emission band peaking at about 384 nm for Ce3+, without the characteristic doublet, are attributed to the extensive crystal-field splitting of 4f ground state. The emission of Gd3+ consists of well-known sharp lines and two weak bands around 319.5 and 325 nm. These bands are due to the coupling of Gd3+ with BO33- groups. The green emission of Tb3+ is considerably sensitized by Ce3+. Energy transfer from Ce3+ to Tb3+ in CaAl2B2O7 is efficient. (C) 1997 Elsevier Science Ltd.

The fabrication of dipped CdS and sputtered ITO thin films for photovoltaic solar cells

Stable bilayer thin films of indium tin oxide (ITO) on CdS and CdS on ITO were formed for the window material of solar cells by chemical bath and sputtering methods. Scanning electron microscopy and X-ray diffraction studies have shown that both the ITO and CdS films are continuous, homogeneous, with high compactness. Measurement of the CdS film thickness across the 2 x 4 cm(2) reveals the good uniformity of these films. Four-point probe measurements show that the resistivity of a CdS film on an ITO surface is much better than that of the single CdS film The thermal stability of an ITO/CdS bilayer, interfacial reaction and optical transmittance were investigated at different annealing temperatures and environments (air, vacuum and N-2 + H-2). The results showed that the ITO/CdS bilayer film is a good window material for the CuInSe2 and CdTe cells. It is a simple method using a small amount of the cadmium compound.

STRUCTURE AND PROPERTIES OF POLYVINYL-ALCOHOL AMIDOXIME CHELATE FIBER

Polyvinyl alcohol amidoxime (PVAAO) chelate fiber prepared in our laboratory is a good adsorbent. Comparing with other adsorbents, it has many advantages, such as higher hydrophilicity, better adsorbability and easier synthesis. In this work, the synthesi

PHASE-BEHAVIOR IN THERMOTROPIC LIQUID-CRYSTALLINE POLYMER AND POLYARYLETHERSULFONE BLENDS

An experimental study of the phase morphology and miscibility of binary blends of poly-arylethersulfone (PES) and a liquid crystalline polymer (LCP) of p-oxybenzoate and ethylene terephthalate units in a 60/40 molar ratio (PET-60PHB) is described. Blends

晶体热膨胀与化学键的关系

本文建立了晶体线膨胀系数与化学键参数的经验关系:α=A(RN)/Zexp(Bfi)(其中 A、B 为常数,R 为键长,N 为配位数,Z 为电价,f_i 为离子性)。运用于碱金属卤化物、碱土金属硫族化合物的计算结果与实测值相一致;运用于其它二元晶体也得到合理的结果。另外对热膨胀其它影响因素也作了讨论。

含Eu~(3+)复合钛钽氧化物的研究

研究了TiO_2-Ta_2O_5-Li_2O:Eu~3+体系,当化学通式为Ti_(1-4x-y)Ta_(3x)Li_xO_2:Eu_y~(3+),在0.1≤y≤0.25,0.05

本征及掺杂态聚甲苯胺能带结构计算

本文通过聚(o~-,m~-)甲苯胺本征态及掺杂态共五种模型电子能带的计算,讨论了聚(o~-,m~-)甲苯胺的导电机制,认为聚甲苯胺中主要的载流子为共振的极化子。在计算中将聚甲苯胺视为准一维体系,采用EHMO-CO半经验计算方法。

浓水溶液的膜蒸馏行为——Ⅱ.蒸气压下降和透析作用的影响

膜蒸馏的蒸馏通量随溶液浓度的增加而逐渐降低,其实质是传质分数和组件的蒸馏效率随浓度增大而下降。本文近似地计算了理论传质分数,实际透过分数和组件的蒸馏效率在不同温度条件下的变化情况以及浓度变化对它们的影响,从中分析了浓溶液的蒸气压下降对膜蒸馏的影响,讨论了膜蒸馏过程中因渗透压而产生的透析现象的存在以及透析现象对膜蒸馏的干扰作用。