用扫描电镜研究工程塑料的断裂行为

本文研究了工程塑料——聚碳酸酯及聚对苯二甲酸丁二醇酯的微观断裂行为。研究中采用了静载和动载破断实验,用扫描电镜观察断裂形态特征,并结合宏观力学试验过程分析其断裂行为。实验结果表明,热塑性工程塑料,在加载速率及环境温度固定条件下,其微观断裂行为受材料损伤体积空间分布的影响,材料损伤体积宏观空间分布范围宽,则大分子相互协同动作强,应变均匀,微观塑性形变差别小,断口表面趋于平坦;反之,大分子相互协同动作差,应变易于集中,微观塑性形变差异大,断口表面高低起伏大。     

Formation of 1-(2-aminophenyl)-5-ethoxy-4-methyl-3-phenylpyrazole and 4-methyl-3-phenylpyrazolo-[5,1-b]benzimidazole via an unusual enzotriazole ring opening

Successive treatment of N-[(1-ethoxy)alken-2-yl]benzotriazoles VII with butyllithium and trimethylsilyl chloride in TH-Fat — 78°C followed by refluxing in acidic acetone generated ring-opened 1-(2-aminophenyl)-5-ethoxy-4-methyl-3 phenylpyrazole VIII and 4-methyl-3 phenylpyrazolo[5, 1-b]benzimidazole IX.Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 775–780, June, 1996. Original article submitted May 14, 1996.     

Polycyclic heteroaromatics from reactions of acylbenzotriazoles with aryl isocyanates

N-Acylbenzotriazoles react with aryl isocyanates to form, depending on the type of acyl group, compounds based on five different classes of polycyclic heteroaromatics. Higher alkanoyl-, acetyl-, acetoacetyl-, aroyl-, and cinnamoylbenzotriazoles yield, respectively, derivatives of quinoline, pyrimidino[5,4-c]quinoline, benzo[b]-1,8-naphthyridine, phenanthridine, and indolo[2, 3-b]quinoline by incorporating 3, 3, 4, 2, and 2 molecules, respectively, of the isocyanate per acylbenzotriazole molecule.     

Tautomerism and Rotamerism in 2-(2-Phenylhydrazino)pyridine

The title compound is shown by X-ray crystallography and NMR spectroscopy to exist both in the solid state and in solution as such. Deuterium-induced shifts confirm the phenylamino structure for 2-phenylaminopyridine.     

Inverted Region in Intermolecular Electronic Energy Transfer

A critique of some recent publications (concerning the so-called inverted region in exchange-induced electronic energy transfer) is presented. It is first pointed out that the phenomena reported therein have in fact been known for nearly two decades; next, a derivation of the expression (used in the aforementioned communications) for k _EnT, the transfer rate constant, is presented; finally, it is stressed that this formula cannot provide reliable quantitative predictions.     

"One-pot" tandem C-H borylation/1,4-conjugate addition/reduction sequence

A microwave-assisted, one-pot, iridium-catalyzed aromatic C-H borylation/rhodium-catalyzed 1,4-conjugate addition sequence provides a highly robust protocol suitable for high-throughput array synthesis. Selective formation of either β-aryl-substituted ketones or the corresponding alcohols can be achieved in good overall yields by simple variation of the reaction conditions.     

Silver(I) complexation of linked 2,2'-dipyridylamine derivatives. Synthetic, solvent extraction, membrane transport and X-ray structural studies

Synthesis of the 2,2'-dipyridylamine derivatives di-2-pyridylaminomethylbenzene 1, 1,2-bis(di-2-pyridylaminomethyl)benzene 2, 1,3-bis(di-2-pyridylaminomethyl)benzene 3, 2,6-bis(di-2-pyridylaminomethyl)pyridine 4, 1,4-bis(di-2-pyridylaminomethyl)benzene 5, and 1,3,5-tris(di-2-pyridylaminomethyl)benzene 6 are reported together with the single-crystal X-ray structures of 2, 3, and 5. Reaction of individual salts of the type AgX (where X = NO(3)(-), PF(6)(-), ClO(4)(-), or BF(4)(-)) with the above ligands has led to the isolation of thirteen Ag(I) complexes, nine of which have also been characterised by X-ray diffraction. In part, the inherent flexibility of the respective ligands has resulted in the adoption of a range of coordination arrangements. A series of liquid-liquid (H(2)O/CHCl(3)) extraction experiments of Ag(I) with varying concentrations of 1-6 in the organic phase have been undertaken, with the counter ion in the aqueous phase being respectively picrate, perchlorate and nitrate. In general, extraction efficiencies for a given ionophore followed the Hofmeister order of picrate > perchlorate > nitrate; in each case the tris-dpa derivative 6 acting as the most efficient extractant of the six systems investigated. Competitive seven-metal bulk membrane transport experiments (H(2)O/CHCl(3)/H(2)O) employing the above ligands as the ionophore in the organic phase and equimolar concentrations of Co(II), Ni(II), Zn(II), Cu(II), Cd(II), Pb(II) and Ag(I) in the aqueous source phase were also undertaken, with transport occurring against a pH gradient. Under the conditions employed 1 and 5 yielded negligible transport of any of the metals present in the source phase while sole transport selectivity for Ag(I) was observed for 2-4 and 6.     

Nachweis und Bestimmung des Eisens, sowie seine Trennung von anderen Elementen

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