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In this thesis, a series of complexes based on aromatic multicarboxylic acids have been successfully synthesized in solutions or under hydrothermal conditions. Their structure and properties are investigated.(1) Eight complex compounds have been synthesized and characterized by X-ray single crystal diffractive technology: The eight complexes are listed as following: [Cu242] complex 1 [Cd22(H2O)4]·4H2O complex 2 [Co(H2btc)(H2O)3] complex 3 [Co2(H2O)2]·H2O complex 4 [Ni22(H2O)4] complex 5 [Cu22(H2O)4] complex 6 [Co(H2biim)2(H2O)2](H2btc) complex 7 [Zn(H2biim)2(H2O)2](H2btc) complex 8 The structure of complex 1 is dinuclear complex resulted from weak interactions(0-D chain); complex 2 is 1-D chain stucture result from interactions of water molecules; complex 3、4、5、6 are coordination polymers using hydrothermal synthses, where the first kind ligand is H4btc, the second kind ligand is phen and Co2+、Ni2+、Cu2+ as center ions, respectively. While the coordination enviroment of Co2+ is the same in complex 3, the coordination geometries around the Co atoms in complex 4 are obviously different because of the different reaction conditions. In complex 4, the 1-D chains are connected into 2-D layer through carboxy groups of ligand H4btc. The structures of complex 5、6 are 1-D chain stucture result from interactions of carboxy groups in ligand H4btc. Complex 7、8 are homeomorphy compounds. Either of them are linked to the 3-D chains through intermolecular hydrogen bonds. Each H4btc lose two protons and H2btc2- acts as negative electron balance.

合成了8个结构新颖的配合物,并用X-射线单晶结构分析方法确定了晶体结构,分别为: [Cu242] 配合物1 [Cd22(H2O)4]·4H2O 配合物2 [Co(H2btc)(H2O)3] 配合物3 [Co2(H2O)2]·H2O 配合物4 [Ni22(H2O)4] 配合物5 [Cu22(H2O)4] 配合物6 [Co(H2biim)2(H2O)2](H2btc)配合物7 [Zn(H2biim)2(H2O)2](H2btc)配合物8 配合物1是一个依靠弱作用连接的双核铜结构;配合物2借助水分子形成一维链状结构;配合物3、4、5、6是以H4btc为第一配体、phen为第二配体,通过水热法合成的配合物,其中,Co2+、Ni2+、Cu2+为中心离子;配合物3中的二价钴离子具有相同的配位环境,不同反应条件下得到的配合物4中的二价钴离子存在不同的配位环境,在配合物4中,一维链通过H4btc上的羧基形成一个二维层结构;配合物5、6是借助H4btc上的羧基形成的一维链状结构;配合物7、8属于异质同晶结构,它们的分子通过分子间氢键形成三维网状结构,H4btc上的羧基失去2个质子,作为一个二价负离子起到电荷平衡作用。

The article has researched occupation of ions in jadeite, diopside and omphacite in jadeite jade on the base of 222 components data. The author has calculated all theie formula and testified that ∑ and ∑ should be positive correlation.

以222点电子探针的化学成分为依据,研究了翡翠中重要组分矿物硬玉、绿辉石和钠铬辉石的离子占位,离子间交换规律等,着重讨论了透辉石—绿辉石—硬玉固溶体系列的类质同象替换,并通过对所有成分点的晶体化学式的计算,验证了∑与∑呈正相关等理论。

On the other hand, Pb~ coordination polymers with 1,4-nda and 2,6-nda exhibit the distinct 3-D 5-connected network and 3-fold interpenetrated diamond framework, revealing the isomeric effect of such tectons.

另外萘二酸的同分异构效应对晶体结构的影响可以在两个由1,4-nda和2,6-nda构筑的pb~化合物中看出(5和6),它们表现出截然不同的5-连接三维结构和三重互穿金刚石拓扑结构。

Progress of recent studies on the deformation mechanism for spherulites of isotactic polypropylene in the uniaxial and biaxial orientation process was introduced.

介绍了近来国内外对单向、双向拉伸过程中全同立构聚丙烯晶体内部球晶形变机理的研究进展。

The existence of such centers. is attributed to defects in crystals resulting from isomorphism between cations of different valences.

阳离子不等价类质同象造成的晶体缺陷,是使其具有电子-空穴心的内在因素。

In the same experimental condition, three 5-at% Yb3+-doped crystals were tuned using one fused quartz. The range of their tunable wavelengths are 70 nm,66 nm and 74 nm, respectively.

三块掺杂率均为5%的Yb3+激光晶体Yb:LSO、Yb:GSO和Yb:GYSO在完全相同的实验条件下由同一块熔融石英棱镜实现了可调谐激光的输出,调谐范围分别为70 nm、66 nm和74 nm。

The crystalline body of the enzyme had been attained in the Turku biological technology center, Finland.

由芬兰Turku生物技术中心完成该酶的晶体结晶,为今后该酶三维空间结构的分析和同类型酶蛋白的结晶打下了基础。

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