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For Pb-based cold fusion reactions to form super heavy nuclei, the optimal excitation energy, the capture cross-section to form a DNS, the compound nuclear formation probability, and the survival probability are calculated.

对一些以Pb为靶的形成超重核的冷熔合反应,计算了最佳激发能、形成双核系统的俘获截面、复合核形成几率及存活几率等,所得到的形成超重核蒸发剩余截面与已知实验值符合较好。

Results We found that (1) at 0 Gy, MN yield was 11.3 ± 2.7 per 1000 binucleated cells.

结果 (1)在 0 Gy时,每 10 0 0个双核细胞的微核量是 11.3± 2 。7,人参水提取物≥ 5 0 0μg· ml- 1 时微核量下降,但微核量和人参水提取物的浓度之间的差异是显著的。

In high definition and real-time dualcore embedded systems for catadioptric omnidirectional imaging, the dual-core DMA communication method was used to provide high speed panoramic data communication between DSP and FPGA.

提出基于逆向波形分析的方法,实现DSP与FPGA之间的双核DMA通信,用于满足高分辨率、实时折反射全景成像双核嵌入式系统中DSP与FPGA之间全景图像数据高速传输的需要。

Crystal structural analysis reveals that, because water molecules bond to Cu atoms, the dhbd ligand can only adopt a hydroxyl oxygen atom to bridge two reversed U-shaped subunits into a novel centrosymmetric dual-U-shaped tetranuclear Cu structure. Each U-shaped frame consists of two crystallographically distinct Cu atoms, two dpphen ligands and one coordinated water molecule.

晶体结构分析表明,由于水的配位阻断, 2,3-二羟基丁二酸根仅通过单羟基氧桥联两个U形双核亚单元形成具有一个对称中心的双U形四核结构,其中U型亚单元包含晶体学上不对称的2个Cu原子、1个2,3-二羟基丁二酸根、2个4,7-二苯基-1,10-邻菲咯啉和1个配位H2O分子。

In the structures of these complexes, zinc can act as the vertex of the networks in various styles: single atom; dicarboxylate, tricarboxylate or tetracarboxylate bridged binuclear SBU ; and octacarboxylate bridged trinuclear SBU.

在这些配合物的结构中,锌离子可以按多种形式作为网络结构的顶点:单原子,双羧基、三羧基或四羧基桥连的双核锌次级结构单元,八羧基桥连的三核锌次级结构单元,再与配体组装成不同的配位聚合物网络。

Six new ligands and 2 mononuclear,5 binuclear,8 tetranuclear complexes all of which are new havebeen synthesised and characterized by elementalanalysis,electric conductance and IR,UV-Vis spactr-oscopic methods.

本文主要研究多核配合物中的磁交换相互作用。共合成了6个新配体,2个单核。5个双核和8个四核配合物,并用元素分析,红外,紫外一可见。

Part 6 explores the reaction system containing O-phthalate, Mn〓 and α,α'-diimine, and yields six novel complexes 16~20 possessing binuclear and tetranuclear matello-crown aether as well as 1-D linear structures, indicating that O-phthalate is a potentially useful ligand to give manganese species in a discrete form.

研究了邻苯二甲酸/锰/双齿亚胺(2,2'-联吡啶和1,10-邻二氮杂菲)的反应体系,合成出6个新颖的双核、四金属冠醚和一维线性结构的化合物16至20,表明邻苯二甲酸是合成有限核数锰簇的有用配体。

Several novel structures have been determined: Unique ninenuclear complexesincorporating 3d, 4f metals with a sodium ion center, the sodium ion may be serve as atemplate in the formation of these novel complexes; Novel tetranuclear 〓complexes with channels formed by intermolecular weak interactions; First 〓type tetranuclear complex; Peculiar "dimer of dimers" complexes derived frombinuclear complex; Unusual one-dimensional wave chain formed by weakcoordination bonds and hydrogen bonds and two dimensional coordination polymerconstructed through coordination bonds and hydrogen bonds.

1获得了多个文献首报和罕见的特殊结构的配合物:两个同时含有碱金属-过渡-稀土金属的独特的九核配合物;两个具有孔道的稀土-过渡金属异四核配合物;草酰胺类〓四核配合物;两个由双核配合物通过叠氮和单个氯原子连成的四核配合物,尤其是以单个氯桥相连的化合物非常少见;一个由弱配键和氢键连成的具有一维波浪形结构的配合物;一个通过配位键和氢键连成的二维配位聚合物。

All synthetic methods of the μ-oxo-bismetallo- tetraphenylporphyrins are comprehensively discussed, involving the two-step method, the chromatographic column method, the one-step method, the auto-oxidation method and the one-pot method developed by our group.

重点介绍了μ-氧代四苯基双核金属卟啉的合成方法,即两步合成法、柱色谱分离法、一步合成法、自氧化法以及本课题组最新开发的一锅法。其中一步合成法和自氧化法由于具有适用范围广、收率高等优点,将成为μ-氧代四苯基双核金属卟啉的主要合成方法。

The ESR data of 3f suggest that Cu〓 is in a distorted tetrahedral field, that is to say, Cu〓 is coordinated to three tertiaty nitrogen atoms and one chloride anion.

为了探测模型化合物中Cu〓的配位情况和几何构型,采用相同的方法合成和表征了杂双核化合物3f,ESR信号结合质谱信息表明杂双核化合物3f中,Cu〓是四配位的,即它与一个C1〓和三个叔铵氮原子配位而处于变形的四面体场中。

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However, as the name(read-only memory)implies, CD disks cannot be written onorchanged in any way.

然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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