辐射式方程的解，氢原子波函数，氢光谱。
软件的使用有助于完善氢光谱实验环节，充实实验内容，提高教学效率。
It is helpful in improving the experiment for hydrogen spectrums, enriching the experimental content and raising teaching efficiency.
他们在春天说，他们希望产生一束反氢激光制造出原子光谱的初步测量器以便它能与常态的氢相比较。
They say that in the spring, they hope to train a laser on the antihydrogen to make a preliminary measurement of the atom's spectrum so that it can be compared to regular hydrogen.
利用元素分析、红外光谱、核磁共振氢谱和激光解析电离飞行时间质谱确证了其组成和结构。
Their chemical structures were confirmed by means of elemental analysis, infared spectra, proton nuclear magnetic resonance spectra and mass spectra.
喇曼光谱研究表明，这种薄膜是典型的无氢类金刚石薄膜。
Raman spectrum study shows that the film has typical pikes of hydrogen free diamond like carbon film.
原子光谱数据是研究原子结构的重要参数，氢及类氢离子是原子物理和量子力学研究的理想体系。
Atomic spectrum data are important parameters to research atomic structure, hydrogen and hydrogen-like ions are idea system to study atomic physics and quantum mechanics.
化合物1的光谱数据以及化合物2的全部氢谱数据均为首次报道。
Spectral data of 1 and complete 1h NMR data of 2 were reported for the first time.
用荧光光谱研究了1，4-二氢吡啶衍生物（1，4-DHP）与小牛胸腺DNA（CT-DNA）的相互作用。
The interaction of the 1,4-dihydropyridine derivative(1,4-DHP) with calf thymus DNA(CT-DNA) was studied by using fluorensence spectroscopy.
首先采用传统自组装方法在氢终止的硅表面上制备了十六烯自组装分子膜，并利用X射线光电子能谱和拉曼光谱技术对自组装膜进行了检测。
First of all, 1-hexadecene self-assembled monolayers was fabricated on hydrogen-terminated silicon surface by traditional way and was checked by XPS and Raman spectrum technology.
通过傅立叶红外光谱和氢核磁谱（1H NMR）测试表明所合成的丙交酯和乙交酯具有环状结构。
The resulted D, L-lactide and glycolide were found to have ring structure by fourier transform infrared spectrometry and proton nuclear magnetic resonance(1H NMR) spectrometry.
合成三种N，N＇-1，4-亚丁基双螺吡喃和双螺恶嗪光致变色化合物，通过红外光谱、核磁共振氢谱及元素分析确证其结构。
Three photochromic N, N'-1,4-tetramethylene bisspiropyran and bisspirooxazine compounds were synthesized. They have been identified by IR spectra, 1H -NMR spectra and elemental analysis;
通过红外光谱、核磁共振氢谱明确了聚合物的组成和结构。
The structure and composition of the copolymer were identified and examined by infrared spectrogram and NMR-H spectrum.
通过红外光谱、核磁共振氢谱、元素分析确证了化合物的结构。
The structures of these compounds are identified by IR, HNMR and elemental analysis.
IR光谱分析同样反映出沥青经催化氧化后分子结构中侧链减少，芳环上的氢减少，整个芳环的缩合程度增加。
Meanwhile IR analysis showed that side chain between molecule and hydrogen of aromatic ring were decreased, condensed degree was increased in catalytic oxidation.
采用光散射技术，促使氢分子产生转动跃迁，得到正氢和仲氢的转动拉曼光谱，其峰位为587。
By using light scattering technique, the transition of rotating energy levels from hydrogen molecular occurs and produced rotating Raman bands for orthohydrogen and parahydrogen are at 587.
聚酰亚胺的结构经红外光谱和核磁共振氢谱确认，并对它的溶解性能、特征粘数、光学性能和热性能等进行了表征。
The structure, solubility, intrinsic viscosity, optical and heat property of polyimides was determined by FTIR, NMR, DSC and TGA et al.
所有目标化合物的结构均经过核磁共振氢谱、高分辨质谱及红外光谱的确认。
The structures of all the newly synthesized compounds were characterized by HRMS, 1H NMR and IR spectroscopy.
并采用氢核磁共振，红外光谱和紫外吸收光谱等手段进行了表征。
The pyrazoles ramification containing dithioether is synthesized by one-step method and characterized by H-NMR, IR and UV-Vis spectra.
采用红外光谱、核磁共振氢谱、质谱等方法对1-(1 -环己烯)基二茂铁的结构进行鉴定，并介绍了一种较为方便的合成方法。
The structure of 1 - (1-cyclohexene) ferrocene is analyzed by IR, 'HNMR, MS and a method of synthesis is introduced in this paper.
本文着重从核磁共振光谱的角度（包括氢核磁共振谱和碳核磁共振谱）来研究多甘醇单甲醚季铵盐的结构。
This paper deals with the structural formula of polyethylene glycol quaternary ammonium by the 13C-NMR and 1H-NMR spectra.
所合成的化合物的结构已由质谱（MS）、红外光谱（IR）、核磁共振氢谱（1H NMR）所证实。
The synthetic compounds structure has been confirmed by 1H NMR, MS and IR.
关键中间体及最终产物的结构经质谱、红外光谱、核磁共振氢谱及碳谱得到确证。
The structures of the key intermediates and target molecule were confirmed by ESI-MS, IR and NMR.
帕米格雷及其衍生物的结构经过核磁共振氢谱、红外光谱、质谱等确证。
The structures of Pamicogrel and its derivatives were confirmed by H-NMR, IR, MS.
结果通过优化条件合成了阿立哌唑，总收率40%，目标化合物的结构经元素分析、质谱、氢谱、红外光谱确证。
The structure of the target compound was confirmed by MS, 1H-NMR, IR spectra and elemental analysis.
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 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.
报道了3- 巯基香豆素的合成方法。经元素分析，红外光谱，核磁共振氢谱和质谱确证了其结构。
The synthetic method for 3 mercaptocoumarin is reported. The structure of this compound has been confirmed by elemental analysis, IR, 1HNMR and MS.
结果化合物的结构经红外光谱、核磁共振氢谱、核磁共振碳谱确证。
Results the chemical structure of the target compound was confirmed by ir, 1h-nmr, 13c-nmr.
产物的结构通过红外光谱、核磁共振氢谱、质谱和单晶x -射线衍射法确定，并提出了可能的反应机理。
The structures of the products were determined by IR, 1h NMR, HRMS and X-ray analysis. And a possible reaction mechanism was put forward.
产物的结构通过红外光谱、核磁共振氢谱和质谱确定。
The structures of the products were determined by IR, 1h NMR and HRMS.
结果与结论罗库溴铵的结构经红外光谱、核磁共振氢谱、质谱、元素分析确证，总收率达24.9%。
Results and conclusion The target compound was identified by IR, 1H-NMR, MS and elemental analysis, the overall yield is 24.9%.
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