The crystal structure has been determined by X-ray single crystal diffraction.
用x -射线单晶衍射测定了其晶体结构。
The products were determined through IR, 1H NMR, MS and X-ray single crystal diffraction.
产物经红外光谱1、H 核磁共振谱、质谱和X射线衍射确定结构。
The crystal and molecular structure has been determined by X-ray single crystal diffraction.
用x -射线单晶衍射测定了该化合物的晶体和分子结构。
Suitable single crystal of hexanitrostilbene(HNS) was cultured and its crystal structure was determined by X-ray single crystal diffraction method.
培养得到六硝基茋（HNS）晶体，应用X-射线单晶衍射法测定了其晶体结构。
A new supramolecular compound has been synthesized under hydrothermal conditions and characterized by element analysis, IR, TG analysis and single-crystal X-ray diffraction.
在水热条件下合成了一种新型超分子化合物，通过元素分析、红外光谱、热重分析和X射线单晶衍射方法确定了其晶体结构。
The title compound C11H10O4 has been synthesized and its crystal structure was determined by single - crystal X-ray diffraction.
标题化合物c11H 10o4的晶体结构用x -射线单晶衍射法测定。
The crystal structure of the compound has been determined by elemental analysis and X-ray single-crystal diffraction.
并通过元素分析及X-射线单晶衍射法，测定了该化合物的晶体结构。
The crystal structure was determined by X ray single crystal diffraction analysis.
用X射线单晶衍射分析法测定了该配合物的晶体结构。
Single crystal X-ray diffraction analysis reveals that the anthracene backbone adopts one of the largest end-to-end twists.
单晶结构分析揭示，其蒽核骨架的扭曲幅度在目前已有报道中属于较大的角度之一。
The crystal structure of the complex was determined by X-ray single diffraction.
用X-射线单晶衍射分析确定了其晶体结构。
The lattice perfection of the InAs single crystal is studied with X-ray diffraction.
利用X射线双晶衍射分析了晶体的完整性。
Two novel divalent transition metal disulfonates were synthesized and characterized by X ray single crystal diffraction.
合成了两个二价的过渡金属磺酸化合物，并通过X -射线衍射单晶结构分析进行结构表征。
The single crystal of HEDP was obtained through recrystallization method, which was characterized by single crystal X-ray diffraction technique, infrared and NMR spectroscopy.
用重结晶方法得到了羟基乙叉二膦酸的单晶，通过单晶x -射线衍射技术测定了晶体的结构，并用红外光谱和核磁共振波谱对其进行了表征。
By IR, elemental analysis and single crystal X-ray diffraction the complexes (1-4) were characterized.
通过红外、元素分析和单晶x -射线衍射对配合物(1 - 4)进行了表征。
The crystal structure was determined by X ray single crystal diffraction, the structure is a distorted triangular bipyramid with five coordinated central tin atom.
用X射线单晶衍射测定了该配合物的晶体结构。结果表明，配合物中锡原子呈五配位畸变三角双锥构型。
The crystal structure has been determined by X ray single crystal diffraction, showing a distorted trigonal bipyramidal configuration with five coordination for the central tin atom.
通过元素分析、 红外光谱和氢核磁共振谱对其结构进行了表征。用X-射线单晶衍射测定了该化合物的晶体结构。
The technical progress on X-ray diffraction for single crystal during last ten years was reviewed.
本文评述了十余年来单晶X射线衍射技术的进展。
The crystal structures have been determined by single-crystal X-ray diffraction.
所有化合物的晶体结构都通过单晶X-射线衍射确定。
Both the compounds are determined by single crystal structure X-ray diffraction and characterized by IR spectra, TG, elemental analyses and XRD.
两个化合物都通过X -射线单晶衍射确定了它们的结构，并通过IR光谱，TG，元素分析和XRD对它们进行了表征。
A serials of complexes of chrysin and its sulfonate derivates were synthesized. And the structures were characterized by spectra and X-ray single-crystal diffraction analysis.
一系列白杨素及磺化衍生物的配合物已被合成，其结构通过光谱手段和x射线单晶衍射确定。
The crystal structure of the substituted cucurbituril has been detected by using single crystal X-ray diffraction analysis.
方法用多种色谱技术对化合物进行分离纯化，并用光谱技术和单晶X射线衍射技术鉴定化合物的结构。
The crystal structure of the substituted cucurbituril has been detected by using single crystal X-ray diffraction analysis.
方法用多种色谱技术对化合物进行分离纯化，并用光谱技术和单晶X射线衍射技术鉴定化合物的结构。
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