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961.
962.
963.
Generalized elasticity theory of quasicrystals 总被引:1,自引:0,他引:1
964.
965.
966.
967.
A new self-assembled and highly oriented one-dimensional single-crystal nanostructure of WO3 with hexagonal form was successfully prepared by a mild, solution-based colloidal approach. 相似文献
968.
Lithiation of diarylbenzotriazol-1-ylmethanes followed by addition of copper( I ) iodide gave 6-arylphenanthridine derivatives in moderate yields. When the two aryl groups were the same or contained very different electron densities, only one product was obtained. However, when the two aryl groups exhibited electron densities of similar magnitude, two isomers were afforded. According to the substituent effect, we believe that the reactions proceed via radical intermediates formed by copper( I ) iodide. 相似文献
969.
笼形聚偕胺肟树脂的研究—酚处理对树脂吸附贵金属性能的影响 总被引:5,自引:0,他引:5
研究了笼形聚偕胺肟树脂(CAO)和酸式(ACAO)及碱式(BCAO)树脂对于苯酚、对-氨基酚、对-硝基酚、对-甲氨基酚和对-苯二酚的吸附和吸留作用,测定了酚处理树脂的中和当量。它反映了笼形树脂吸留外来物的特性。酚处理树脂有效地吸附Ag 、AuCl4-、PtCl62-、PdCl42-和IrCl62-等贵金属离子,吸附方式似乎与溶液的pH值有关。SEM观察表明,Ag 、Au-Cl4-和IrCl62-离子在吸附过程中被还原为零价态,在树脂表面生成形态各异的结晶。 相似文献
970.
Photoinduced reactions of chloranil with 1,1-diarylethenes and product photochemistry-intramolecular 总被引:1,自引:0,他引:1
Photoinduced reactions of chloranil (CA) with 1,1-diarylethenes 1 [(p-X-Ph)(2)C=CH(2), X = F, Cl, H, Me] in benzene afforded products 4-14, respectively, with the bicyclo[4.2.0]oct-3-ene-2,5-diones 4, the 6-diarylethenylcyclohexa-2,5-diene-1,4-diones 5, and 2,3,5, 6-tetrachlorohydroquinone 13 as the major primary products. The cyclobutane products 4 are formed via a triplet diradical intermediate without involvement of single electron transfer (SET) between the two reactants, while 5 is derived from a reaction sequence with initial SET interaction between (3)CA and the alkene. The 9-arylphenanthrene-1,4-diones 6 and its 10-hydroxy-derivatives 7 are secondary photochemical products derived from 5. The isomeric cage products 9-11 are formed from 4 via intramolecular benzene-alkene [2 + 2] (ortho-)photocycloadditions induced by the triplet excited enedione moiety. The relative amount of the two groups of products (4 and its secondary products 9-11 via non-SET route vs 5 and its secondary products 6, 7, 8, 12, and 14 via SET route) shows a rather regular change, with the ratio of non-SET route products gradually increasing with the increase in oxidation potential of the alkenes and in the positive free energy change for electron transfer (DeltaG(ET)) between (3)CA and the alkene, at the expense of the ratio of the products from the SET route. The competition between the SET and non-SET routes was also found to be drastically influenced by solvent polarity, with the SET pathways more favored in polar solvent. Photo-CIDNP investigations suggest the intermediacy of exciplexes or contact ion radical pairs in these reactions in benzene, while in acetonitrile, SET process led to the formation of CA(*)(-) and cation radical of the alkene in the form of solvent separated ion radical pairs and free ions. 相似文献