Quantum chemical study on influence of intermolecular hydrogen bonding on the geometry, the atomic charges and the vibrational dynamics of 2,6-dichlorobenzonitrile

FT-IR (4000-400 cm(-1)) and FT-Raman (4000-200 cm(-1)) spectral measurements on solid 2,6-dichlorobenzonitrile (2,6-DCBN) have been done. The molecular geometry, harmonic vibrational frequencies and bonding features in the ground state have been calculated by density functional theory at the B3LYP/6-311++G (d,p) level. A comparison between the calculated and the experimental results covering the molecular structure has been made. The assignments of the fundamental vibrational modes have been done on the basis of the potential energy distribution (PED). To investigate the influence of intermolecular hydrogen bonding on the geometry, the charge distribution and the vibrational spectrum of 2,6-DCBN; calculations have been done for the monomer as well as the tetramer. The intermolecular interaction energies corrected for basis set superposition error (BSSE) have been calculated using counterpoise method. Based on these results, the correlations between the vibrational modes and the structure of the tetramer have been discussed. Molecular electrostatic potential (MEP) contour map has been plotted in order to predict how different geometries could interact. The Natural Bond Orbital (NBO) analysis has been done for the chemical interpretation of hyperconjugative interactions and electron density transfer between occupied (bonding or lone pair) orbitals to unoccupied (antibonding or Rydberg) orbitals. UV spectrum was measured in methanol solution. The energies and oscillator strengths were calculated by Time Dependent Density Functional Theory (TD-DFT) and matched to the experimental findings. TD-DFT method has also been used for theoretically studying the hydrogen bonding dynamics by monitoring the spectral shifts of some characteristic vibrational modes involved in the formation of hydrogen bonds in the ground and the first excited state. The C-13 nuclear magnetic resonance (NMR) chemical shifts of the molecule were calculated by the Gauge independent atomic orbital (GIAO) method and compared with experimental results. Standard thermodynamic functions have been obtained and changes in thermodynamic properties on going from monomer to tetramer have been presented. (C) 2013 Elsevier B.V. All rights reserved.

Spectral characterizations and photophysical properties of one-step synthesized blue fluorescent 4 `-aryl substituted 2,2 `:6 `,2 `'-terpyridine for OLEDs application

We have synthesized a series of 4'-aryl substituted 2,2':6',2 `'-terpyridine (terpy) derivatives, namely 4'-(4-methylphenyl)-2,2':6',2 `'-terpyridine (C-1), 4'-(2-furyl)-2,2':6'2 `'-terpyridine (C-2), and 4'-(3,4,5-trimethoxyphenyl)-2,2':6',2 `'-terpyridine (C-3). The synthesized terpy compounds were characterized by elemental analyses, FTIR, NMR (H-1 and C-13), and ESI-Mass spectrometry. Photophysical, electrochemical and thermal properties of terpy compounds were systematically studied. Maximum excitation band was observed between 240 and 330 nm using UV-visible spectra, and maximum emission peaks from PL spectra were observed at 385, 405 and 440 nm for C-1, C-2 and C-3 respectively. Fluorescence lifetime (tau) of the fluorophores was found to be 035 and 1.55 ns at the excitation wavelength of 406 nm for C-1 and C-2 respectively, and tau value for C-3 was found to be 0.29 ns at the excitation wavelength of 468 nm. We noticed that the calculated values of HOMO energy levels were increased from 5.96 (C-1) to 6.08 (C-3) eV, which confirms that C-3 derivative is more electrons donating in nature. The calculated electrochemical band gaps were 2.95, 2.82 and 3.02 eV for C-1, C-2 and C-3 respectively. These blue fluorescent emitter derivatives can be used as an electron transport and electroluminescent material to design the blue fluorescent organic light emitting diode (OLED) applications. (C) 2015 Elsevier B.V: All rights reserved.

Laser action from 1,3,5,7-tetramethyl-2,6-diethyl-8-n-propyl pyrromethene-BF2

We measured spectroscopic and laser action properties of a novel 8-position substituted pyrromethene-BF2, namely 1,3,5,7-tetramethyl-2,6-diethyl-8-n-propyl pyrromethene-BF2 complex. The laser action was performed with the corresponding dye solution in ethanol, which was placed in a Littman-type laser cavity pumped by the second harmonic of a Q-switched Nd:YAG laser. The spectroscopic measurements clearly indicated that the corresponding dye solution in ethanol exhibited intense absorption in the visible spectral region with large fluorescence quantum yield. It possesses rather low triplet-triplet absorption in the spectral region 460-550 nm and almost negligible triplet-triplet absorption in the lasing spectral region. As a consequence, it lases nearly as efficiently as commercially available benchmark laser dyes such as Rhodamine-6G and outperformed them in wavelength tunability in our laser cavity and pump geometry. (C) 2002 Optical Society of America.

黄土高原陇东盆地朝那红黏土8.1～2.6 Ma的孢粉记录

IEECAS SKLLQG

~(206)At的[лh_(1/2)vi_(13/2)~(-1)]10~-同质异能态研究(英文)

利用能量为６０－８０ＭｅＶ的~(１２)Ｃ束流，通过~１９７Ａｎ（~(１２)Ｃ，３ｎ）~２０６Ａｔ反应研究了~２０６Ａｔ核的高自旋能级结构．用７台ＢＧＯ（ＡＣ）ＨＰＧｅ探测器和一台用于探测低能γ射线的平面型ＨＰＧｅ探测器进行了γ射线的激发函数、γ－γ－ｔ符合及γ射线的角分布测量．基于这些测量，首次建立了包括２５条γ跃迁的~２０６Ａｔ高自旋能级纲图．确定了一个半寿命为（９０８±４００）ｎｓ、自旋和宇称为１０的同质异能态．基于较重的双奇核~(２０８，２１０ )Ａｔ能级结构的系统性，对~(２０６)Ａｔ的１０~－同质异能态进行了讨论．

The first soluble conjugated poly(2,6-anthrylene): synthesis and properties

The first soluble conjugated poly(2,6-anthrylene) with 9,10-diphenyl-anthracene as the repeating unit is reported; photophysical studies reveal that this polymer represents a novel well-conjugated system.

La_2CaB_(10)O_(19)∶Eu~(3+)的VUV-VIS范围光谱的研究

研究了La2CaB10O19∶Eu3+红色发光材料的高分辨发射光谱和UV VUV激发光谱。根据发射光谱和荧光寿命,认为进入晶格的Eu3+占据了两种格位,一种Eu3+占据了与O2-离子十配位的La3+的格位,另一种Eu3+则占据了与O2-离子八配位的Ca2+的格位。又从激发光谱的分析中,得到Eu3+的电荷迁移带(CTB)是峰值位于244nm的宽带,而位于130～170nm之间的成份复杂的宽带包括硼酸盐基质的吸收带和Eu3+的f d跃迁的结论。

Preparation and crystal structures of LaCl3(15-crown-5) and [LaCl2(phen)(H2O)(2)(mu-Cl)](2)center dot(15-crown-5)center dot MeCN

LaCl3(15-crown-5), I was prepared by the reaction of LaCl(3)nH(2)O with 15-crown-5 and bipy (2,2'-bipyridyl). [LaCl2(phen)(H2O)(2)(mu-Cl)](2) .(15-crown-5). MeCN, II, was crystallized from a mixture of LaC1(3) . nH(2)O, phen (1,10-phenanthroline) and 15-crown-5 in MeOH/MeCN, Crystal structures of these two complexes have been determined by X-ray methods. The La(III) ion in I is coordinated by three Cl anions and five oxygen atoms of a crown ether. The two metal ions in II are bridged by two Cl anions and the crown ligand is hydrogen-bonded to the coordinated water molecules to form polymeric... crown/cation/cation/crown... chains.

5，10，15，20－四（对－山嵛酸乙酯－α－氧代苯基）卟啉LB膜结构研究

５，１０，１５，２０－四（对－山嵛酸乙酯－α－氧代苯基）卟啉ＬＢ膜结构研究王海水，曾广赋，谷淑珍，席时权（中国科学院长春应用化学研究所长春１３００２２）利用ＬＢ膜技术将分子组装成有序的分子单层或多层体系，研究膜内分子间相互作用和分子的结构，对了解结构...

（C_（12）H_8）~（2＋）离子中电荷定位的理论研究

本文用半经验量子化学方法ＭＮＤＯ研究了由联苯衍生物产生的［Ｃ１２Ｈ８］２＋双电荷离子的结构，讨论了其中的电荷定位和影响离子稳定性的因素，双电荷离子的两个电荷分别定位于两个苯环上，表明该离子是由联苯衍生物经两步反应产生。

5,10,15,20-四(对-乙酯苯基)卟啉LB膜的结构

对卟啉类化合物LB膜的结构、电性质和气敏性的研究已见报道。本文利用膜天平和UV-Vis分光光度计研究了标题化合物在气-液界面上的成膜特性、分子间相互作用和LB膜的结构。5,10,15,20-四(对-乙酯苯基)卟啉(TPEPP)由5,10,15,20-四(对-氰苯基)卟啉和乙醇酯化得到。元素分析测定值与计算值相符。λ(CHCl_3,nm):421,515,550,590,645;ν(KBr压

马尾藻种群遗传及早期发育的研究

本研究运用RAPD和ISSR两种分子标记技术，对采自山东半岛4个不同地理位置的鼠尾藻（Sargassum thunbergii）和海黍子（S. muticum）种群进行了遗传多样性和遗传结构的研究，从而对其种群间的地理隔离、基因流动水平及其影响因素做出估计和判断，为马尾藻自然资源的保护和开发提供依据。在室内对鼠尾藻有性生殖幼苗的早期发育和生长进行了研究，了解其繁殖生物学特性，为鼠尾藻人工种苗的培育提供依据。主要研究结果如下： 对4个鼠尾藻（S. thunbergii）地理种群的遗传多样性研究中，筛选出了28条RAPD 引物和19条ISSR引物，分别扩增产生了174和125个位点。选用的三种不同指标，即多态位点比率（P％，percentage of polymorphic loci），平均预期杂合度（H，the expected heterozygosity）和 Shannon's 信息多样性指数（I，Shannon's information index），均可反映出鼠尾藻种群内部的遗传多样性呈较低水平。而群体间遗传距离（D，Nei’s unbiased genetic distance）矩阵和固定化指数（FST,the fixation index）矩阵均反映出群体间高度的遗传分化。通过分子变异分析（AMOVA，Analysis of molecular variance）来区分来自种群内部和种群之间的遗传变异，揭示出多数的遗传变异（57.57% 或59.52%）来自于鼠尾藻种群之间。另外，Mantel分析表明，4个鼠尾藻种群间的遗传分化与地理距离呈正相关（r>0.5），遵循传统的IBD（isolation by distance）模式，UPGMA（unweighted pair group method with arithmetic averages）聚类分析也反映出相似的结果。 对4个海黍子（S. muticum）地理种群遗传结构的研究中，筛选出的24条RAPD 引物和19条ISSR引物分别扩增出164和122个位点。遗传多样性评估结果表明，海黍子种群内部存在较低或者中等水平的遗传多样性，而D矩阵和FST 矩阵均显示种群间存在高水平的遗传分化。并且，发现D和FST 矩阵在RAPD和ISSR分析中均具有高且显著的相关性。AMOVA分析显示，种群之间的遗传变异高于种群内部。Mantel分析和UPGMA聚类分析均发现海黍子种群间的遗传分化遵循IBD模式，即与地理隔离呈正相关（r>0.6）。 并且，RAPD和ISSR分析的结果高度一致（r>0.9，P<0.05），均揭示4个海黍子种群之间存在高度的遗传分化。 对鼠尾藻有性生殖幼苗早期生长发育的研究结果表明，其早期发育过程属于马尾藻科（Sargassaceae）中典型的“8核1卵”型。在一定条件下培养两个月后，产生了1～2个小叶，幼苗的长度达2～3毫米。生长实验发现，温度（10, 15, 20, 25℃）和光照强度（9, 18, 44, 88 µEm-2s-1）对培养第一周幼苗的生长均有显著的影响（ANOVA, P<0.01）。在两个月的培养中，幼苗对温度和光强的耐受范围较宽，在10℃～25℃，9～88 µEm-2s-1条件下均可生长，最适温度和光强为25℃，44 µEm-2s-1；低温（10℃）对幼苗的生长有显著抑制。不同光质对幼苗生长的影响显著（P<0.01），相同光强条件下，蓝光和白光相比较，蓝光显然不能满足鼠尾藻幼苗早期生长的需要。