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61.
Yoshiaki Hamada Yoshiaki Amatatsu Masamichi Tsuboi 《Journal of Molecular Spectroscopy》1985,110(2):369-378
The infrared absorption spectrum of 1-aminopropene was observed for the first time in the gas phase. This molecule was produced by the thermal decomposition of cyclopropylamine. Two rotational isomers, cis and trans around the C=C double bond, occur. The relative yield of the conformers depends on the experimental conditions. The main conformer could not be identified experimentally, but an ab initio MO calculation suggests that the trans conformer is a little more stable form than the cis. These empirical assignments of the vibrational modes are supported by the ab initio MO calculation. 相似文献
62.
63.
2-[2-(3,5-Dibrornopyridyl)azo]-5-dimethyIam;nobenzoic acid (3,5-diBr-PAMB) has been synthesized and its potential for the spectrophotometric determination of metals studied. It reacts sensitively with nickel, cobalt, iron and copper, and is particularly useful for nickel. The apparent molar absorptivity in chloroform is 1.50 × 105 l mol-1 cm-1 and the Sandell sensitivity is 0.4 ng Ni cm-2. Nickel reacts with 3.5-diBr-PAMB at pH 4–10; at pH 4–7 the complex can be extracted into chloroform to give a stable purple solution. The optimal calibration range is 0.04–0.4 ppm Ni. Only Cu, Co, Fe, Pd and V interfere seriously but Pd, Cu and V can be masked by thiourea. 相似文献
64.
Takahashi T Tsai FY Li Y Wang H Kondo Y Yamanaka M Nakajima K Kotora M 《Journal of the American Chemical Society》2002,124(18):5059-5067
Selective preparation of pyridine derivatives from two different alkynes and a nitrile was achieved by a novel procedure in which an alkyne and a nitrile couple first to give an azazirconacyclopentadiene followed by reaction with the second alkyne in the presence of 1 equiv of NiCl(2)(PPh(3))(2). This procedure gives only single products of pyridine derivatives from two different symmetrical alkynes and a nitrile. Our novel procedure can be used even with two similar alkyl-substituted alkynes such as 3-hexyne and 4-octyne. Two possible pyridine isomers from 3-hexyne, 4-octyne, and acetonitrile could be completely and independently prepared as single products by this method. The origin of the selectivity comes from the addition order of two different alkynes. This method was applied for the formation of pyridones and iminopyridines using isocyanate and carbodiimide derivatives instead of nitriles, respectively. Reaction of an alkyne with Cp(2)ZrEt(2) and an isocyanate or a carbodiimide gives an azazirconacycle. Treatment of the azazirconacycle with the second alkyne in the presence of 1 equiv of NiCl(2)(PPh(3))(2) gave a pyridone or an iminopyridine derivative. The use of two different unsymmetrical alkynes afforded the pyridine with five different substituents when the first alkyne has a trialkylsilyl group and the second alkyne has a phenyl group as functional groups. On the other hand, azazirconacyclopentadienes reacted with propargyl bromide in the presence of CuCl with excellent regioselectivity to give tetrasubstituted pyridine derivatives as single products. With the assistance of the trialkylsilyl groups, pyridines with all different substituents including H were also prepared. 相似文献
65.
66.
Bis(carbazolylphenyl) and bis(diphenylaminophenyl) derivatives of 1,6-methano[10]annulene, which is luminescent material and contains seven-membered rings, are synthesized. The bis(phenylcarbazole) derivative 3 have high melting point and glass transition temperature. Electroluminescence characteristics of organic light-emitting diodes using these methano[10]annulenes were investigated. 相似文献
67.
An organodisulfide with a pair of adamantane moieties was synthesized, and its self-assembled monolayer (SAM) was formed on Au(111). The adamantane moieties are almost spherical and much bulkier than alkyl chains. The structure was characterized by scanning tunneling microscopy. Two-dimensional crystals of the SAM were found to be four orientationally different hexagonals with almost the same lattice constant with 4 radical 3a/3 and 7a/3 (a = 0.2884 nm, the Au lattice constant). The structure is assigned to four of the high-order commensurate adlayers. The present study of geometry and energetics for self-assembling of such an organosulfur compound with spherical cages provides a new insight into the probable SAM structure of various thiolate derivatives on Au(111). 相似文献
68.
Roles of polymer-solvent complexes in conformational ordering of polymer molecules dispersed in gels
Masamichi Kobayashi 《Macromolecular Symposia》1997,114(1):1-12
On gelation of crystallizable stereoregular polystyrenes (isotactic IPS and syndiotactic SPS), highly ordered skeletal conformations of particular types characteristic of the respective polymer are formed. The conformational orderliness is evaluated in the absolute scale through quantitative analysis of infrared absorption bands due to the respective ordered conformation. The kinetic and/or thermodynamic behaviors of gelation process and the accompanied conformational ordering are strongly influenced by solvent. Solvent effect on the aggregation state formed in SPS gels has been investigated by means of small angle neutron scattering and discussed in relation to the gelation rate. In some solvents, two different ordering processes, gelation and crystallization, proceed in a competitive way. On the basis of these experimental facts, the roles of specific polymer-solvent interactions in gels are considered from the viewpoint of molecular-level structure. 相似文献
69.