单配的

Each Ln ion adopts a dodecahedron coordination environment with eight coordinated oxygen atoms from two terminal monodentate coordinated FcC6H4COO- units, two terminal monodentate coordinated H2O molecules, and fourμ_2-η~2--OOCH_4C_6Fc units.

稀土离子都是八配位的三角十二面体构型，其中两个来自单齿配位的FcC6H4COO-，两个来自配位的水分子，四个来自双齿桥联的μ_2-η~2--OOCH_4C_6Fc。

It crystallizes in the monoclinic space group C2/c, with a=1.6953(3)nm, b=1.9241(4)nm, c=1.7760(4)nm,β=94.75(3)°. Each Gd ion is coordinated by two oxygen atoms from two different radicals NITPh(OCH3)3 and six oxygen atoms from three hfac molecules to form eight-coordinated dodecahedron geometry.

Gd离子采取八配位的模式，两个氮氧自由基作为单齿端基配体分别以氮氧基团的氧原子与Gd离子配位，三个六氟乙酰丙酮阴离子分别以两个氧原子与Gd离子配位，构成十二面体。

The analysis results of crystal structure shows that the stoichiometric mononuclear Ni complex molecule C(subscript 37.5H45Cl2N10O12Ni was composed of two mononuclear Ni complex units {Ni[C35H33N10O](ClO4)2(CH3OH)2.5(H2O)0.5, Ni coordinated to the ligand to form hexacoordinated distorted octahedral configuration, and the orbital contribution and atomic net charge results has provided a good testimony for the coordinated condition in the crystal structure.

晶体结构分析表明，Ni单核配合物的化学经验式C37.5H45Cl2N10O12Ni的单胞中含有两个配合物分子{Ni[C35H33N10O](ClO4)2(CH3OH)2.5(H2O)0.5}，Ni与配位原子形成六配位的扭曲八面体结构。ab从头算所得原子轨道贡献和原子净电荷布居分析结果与晶体结构中的配位情况相符。

Main job is to guarantee the scraping interaction and equipment on both sides of the friction surface or can obtain higher precision and accuracy, precision and shape accuracy, precision and contact transmission because of good lubrication, manual and repeatedly is worthy, large amounts of wind, time-consuming, scraping the time needed for different devices vary, such as boring slider and slide block wind profiling, between the match before measuring clearance between the original value, and then according to the technical requirement to measure the value of time and scraping scraping, then apply DanFen red on the slider, manual let slip on the slide seat back and forth, they do straight-line movement between full contact and friction, reoccupy scraper scraping friction creates the contact point, so repeatedly, until the technical requirements for the match, single within 2 days, must blow to the boring if all the time to work with wind, a half month is required.

刮削过程。刮削工作主要是为了保证设备相互接触并摩擦的两面间能获得较高的尺寸精度、形状精度、位置精度、接触精度、传动精度和良好的润滑，因是手工操作且需反复配刮，故工作量大，耗时较长，设备不同，刮削所需时间也各不相同，例如镗床上滑座与下滑座间的配刮，刮削前先测量出二者之间原有的间隙值，然后根据工艺要求测算出需刮削值及每次的刮削量，再将红丹粉涂于上滑座之上，手工让上滑座在下滑座上来回做直线运动，使它们之间充分接触和摩擦，再用刮刀刮削摩擦产生出的接触点，如此反复多次，直至技术要求范围之内，单此项配刮需2天左右，若对于整个镗床所有配刮工作的时间总和，则需半个月左右。

The result is that both tin atoms are five-coordination, have a distorted trigonal bipyramidal geometry with an additional week interaction between another oxygen atom and tin atom.

分子中四个羧酸酯基有桥联双齿和单齿两种不同的配位模式；在内环锡和外环锡的配位单元中，锡均形成具有五配位的畸变三角双锥配位构型，同时另有一氧原子与中心锡原子之间有弱相互作用。

Two qina ligands chelate a cobalt ion by 0 and N atoms and two DMSO ligands coordinate a cobalt ion by two O atoms at an axis. The complex formed inerratic octahedron configuration, and π-π stacking weak interaction was observed between the molecules.

配合物为单斜晶系，P2(1)/C空间群，2个qina配体以氮原子和氧原子与Co离子螯合配位，2个DMSO以氧原子与Co离子轴向配位，形成规则的八面体构型配合物，分子之间存在π-π堆积弱相互作用。

Following evidences indicate that lherzolite and garnet pyroxenite xenoliths in basalts are captures of mantle fragments when host magma ascending: crystallizing temperatures and pressures of cpx megacrysts and some phenocrysts in host magmas are greater than equilibrium temperatures and pressures of xenoliths; calculated REE partition pattern of assumed equilibrium melts is not comparable with that of studied host basalt rocks; olivine in xenoliths is not in equilibrium with basalt rocks.

寄主玄武岩的单斜辉石斑晶—熔体平衡温度高于石榴石二辉橄榄岩和石榴石辉石岩包体的平衡温度，单斜辉石巨晶和部分斑晶—熔体平衡压力大于包体平衡压力，寄主碱性玄武岩的稀土配分型式和所计算的与尖晶石二辉橄榄岩包体平衡的熔体的稀土配分型式不同，包体橄榄石与寄主岩浆之间的Fe-Mg交换系数低于0.30，均表明包体与寄主玄武岩浆之间不存在平衡关系，因此，包体是被寄主玄武岩浆捕虏的上地幔碎块。

The results are following:(1)We investigated the influence of the positional isomeric effect on structures.Due to the less space-crowding,it is easier for 3-pytpy to behave as bridging ligand than 2-pytpy under the same reaction conditions,while,it is easier for 2-pytpy to function as tridentate chelating ligand to construct supramolecular structures.

研究结果如下：(1)研究了两个吡啶取代三联吡啶配体的位置异构效应对配合物结构的影响。3-pytpy配体比2-pytpy具有更小的空间位阻，在相同的合成条件下容易以单-三齿桥联方式配位；而2-pytpy更易以三齿螯合形式配位，通过π…π堆积作用形成超分子结构。

It was found that the central metal ion is located at the symmetric center of the molecule. Four oxygen atoms from two H2O molecules and two 〔C6H4(CO2)2〕2- groups are coordinated with copper ion to form a similar planar square coordination configuration. There is one only unidentate coordination bond between O(1) in 〔C6H4(CO2)2〕2- and Cu2+.

结构分析发现，中心金属离子位于分子的对称中心位置，铜离子与来自2个水分子和2个邻苯二甲酸根中的4个氧原子形成近似正方形平面配位，邻苯二甲酸根是以1个O(1)与Cu2+离子形成单齿配体，O(2)和Cu2+之间没有形成配位键。

Mn(H_3biim)_2_2Cl_2 and Cd(H_3biim)_2_2Cl_2 have been synthesized from H_2biim, their structures were determined by X-ray crystallography. The two complexes have similar structures and both are neutral compounds. One N atom in H_2biim is protonated, forming a H3biim+ cation. The later is an unidentate ligand, the central metal, Cd or Mn is six coordinated and adopts a distorted octahedral environment.

合成了联咪唑锰配合物Mn(H_3biim)_2_2Cl_2和联咪唑镉配合物Cd(H_3biim)_2_2Cl_2，晶体结构表明这两个配合物结构相似，均为中性化合物，联咪唑的一个氮原子被质子化，形成一价阳离子(H_3biim~+)，它采取单齿配位，中心Mn原子是六配位，其配位环境为畸变的八面体。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。