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2016级硕士生“计算机在化学与材料科学中的应用”试题一、在线和离线虚拟打印机有哪二种?说明超星图书在线和离线虚拟打印转换为PDF文件的方法。(20分)答:离线打印虚拟打印机为PDFFactory,在线虚拟打印机为PDFXChange。超星图书在线和离线虚拟打印转换为PDF文件的方法:离线打印:步骤一:设置虚拟打印机(1)、安装pdffactory;(2)、安装完成后,会发现电脑里多了一个打印机pdffactoryprinter,右键将其设置为默认打印机,然后将名字改为标准打印机或者standardprinter;3.在这个打印机属性设置里,将输出格式设为A4,分辨率为720dpi。步骤二:虚拟打印转换文件(1)、用超星阅览器打开要换的书,先快速过一遍,如果有加密页,将pdg11拷入本书文件夹下解密;(2)、在阅览器图书菜单下选择打印,如果该选项是虚的,在打开的页面上右键选择;(3)、按照正文业和目录页分开打印,打印页数可以参照图书简介里的页数。封面、版权、序言等等附属页,用阅览器打开后分页打印。步骤三:手工合成(1)、安装acrobat;(2)、将上个步骤里分别生成的pdf文件用acrobat的插入功能合并成一个文件,保存。在线打印:(1)、必须保证你的电脑安装了AdobeAcrobatProfessional7.0版本或者更高的版本。超星软件我用的是浩瀚图书馆版4.0.(2)、在打印之前必须先更改打印机设置。打开“控制面板”----“打印机和传真”----将“AdobePdf”打印机的名字改为“PDF打印机”(这属随便取名)即可。(3)、打开你需要打印的超星书籍第一页,点右键选择“打印....”,在弹出的打印设置对话框中,打印范围选择“从当前页开始打印”,并在框中输入页码1(一般默认页码1,不需要输入);在打印页码中输入你下载的该超星文件的文件总个数(一般要比总文件个数大,页码大一些没关系,英文它只是不断重复打印空白页,最好也只是比原来的书多一页空白而已)。设置完毕后点击确定。(4)、在弹出的打印对话框中选择PDF打印机,点击确定,然后选择打印文件的存储位置就开始打印了。二、下载石墨烯制备方面CNKI、维普、万方数据电子期刊各一篇并附首页。(20分)CNKI查询步骤进入之后输入石墨烯制备—点击检索万方输入石墨烯制备—检索首页维普输入石墨烯制备—检索三、美国专利下载可用什么软件?下载美国专利一份并附首页。(20分)DIP-JforUSP四、用Origin绘图软件绘制一张同X轴、不同Y轴2曲线二维图。(20分)五、用CHEMOFFICE绘出下列分子式,模拟其1H、13CNMR,并用MOPAC,PM3计算方法先能量最低化,再计算其生成热,基态偶极矩,、、(Polarizabilities)值。(20分)NSHOOCCOOHCH3分子式用chemoffice—选择选择--接着选择-----------run得到分子式以及生成热,基态偶极矩,、、(Polarizabilities)值:Warning:ArbitrarydihedralchosenforC-C-C-CC(2)-C(3)-C(8)-C(11)Iteration1HeatofFormation:-32.99309GradientNorm:960.950Iteration21HeatofFormation:-113.23564GradientNorm:216.571HeatofFormation:-113.23564kcal/moleDipole:1.6914.8061.093Magnitude:5.211DebyeO(16)PolarizabilitiesO(16)O(16)PolarizabilitiesO(16)H(29)Polarizabilities0.00000eVH(29)O(16)PolarizabilitiesO(16)H(35)AlphaXX:314.47340AUH(35)H(35)AlphaYY:175.19108AUH(35)H(35)AlphaZZ:61.13615AUH(35)O(16)PolarizabilitiesO(16)H(35)BetaXXX:-6318.34803AUH(35)H(35)BetaYYY:140.00613AUH(35)H(35)BetaZZZ:10.25663AUH(35)O(16)PolarizabilitiesO(16)H(27)GammaXXXX:1053343.34077AUH(27)H(31)GammaYYYY:13450.36517AUH(31)H(31)GammaZZZZ:2023.98978AUH(31)O(16)PolarizabilitiesO(16)H(29)Polarizabilities0.25000eVH(29)O(16)PolarizabilitiesO(16)H(35)AlphaXX:315.55621AUH(35)H(35)AlphaYY:175.43694AUH(35)H(35)AlphaZZ:61.20338AUH(35)O(16)PolarizabilitiesO(16)H(35)BetaXXX:-6563.90777AUH(35)H(35)BetaYYY:141.34385AUH(35)H(35)BetaZZZ:10.14746AUH(35)O(16)PolarizabilitiesO(16)H(27)GammaXXXX:1164256.02944AUH(27)H(31)GammaYYYY:13785.85356AUH(31)H(31)GammaZZZZ:2080.60852AUH(31)O(16)PolarizabilitiesO(16)H(29)Polarizabilities0.50000eVH(29)O(16)PolarizabilitiesO(16)H(35)AlphaXX:318.87462AUH(35)H(35)AlphaYY:176.17908AUH(35)H(35)AlphaZZ:61.40784AUH(35)O(16)PolarizabilitiesO(16)H(35)BetaXXX:-7399.95744AUH(35)H(35)BetaYYY:145.62027AUH(35)H(35)BetaZZZ:9.76450AUH(35)O(16)PolarizabilitiesO(16)H(27)GammaXXXX:1629159.20718AUH(27)H(31)GammaYYYY:14869.64176AUH(31)H(31)GammaZZZZ:2270.63913AUH(31)NSOOHOOH6.537.117.102.852.857.52.3511.011.0ChemNMRH-1EstimationEstimationQuality:blue=good,magenta=medium,red=roughProtocoloftheH-1NMRPrediction:NodeShiftBase+Inc.Comment(ppmrel.toTMS)CH6.537.261-benzene0.061-C*R-0.121-C-0.671-N(C)CCH7.117.261-benzene0.221-C*R-0.191-C-0.181-N(C)CCH7.107.261-benzene0.221-C*R-0.201-C-0.181-N(C)CCH32.850.86methyl1.991alpha-N(C)-1:C*C*C*C*C*C*1CH32.850.86methyl1.991alpha-N(C)-1:C*C*C*C*C*C*1CH7.56.962-thiophene0.081-C(=O)O?1unknownsubstituent(s)?1unknownsubstituent(s)from2-furan0.481-C(=O)O-1increment(s)notfoundCH32.350.86methyl1.491alpha-1:C*C*C*C*C*C*1OH11.011.00carboxylicacidOH11.011.00carboxylicacid0246810PPMNSOOHOOH114.7125.4123.2131.3127.5147.3147.940.640.6125.2133.5128.716.1162.6163.4ChemNMRC-13EstimationEstimationQuality:blue=good,magenta=medium,red=rough020406080100120140160180PPMProtocoloftheC-13NMRPrediction:NodeShiftBase+Inc.Comment(ppmrel.toTMS)CH114.7128.51-benzene0.51-C*R-0.11-C-15.41-N(C)C1.2generalcorrectionsCH125.4128.51-benzene-1.51-C*R-3.01-C0.91-N(C)C0.5generalcorrectionsC123.2128.51-benzene8.01-C*R-0.11-C-10.51-N(C)C-2.7generalcorrectionsCH131.3128.51-benzene-1.51-C*R0.71-C0.91-N(C)C2.7generalcorrectionsC127.5128.51-benzene0.51-C*R9.21-C-15.41-N(C)C4.7generalcorrectionsC147.3128.51-benzene0.01-C*R0.71-C16.01-N(C)C2.1generalcorrectionsC147.9125.62-thiophene7.91-C(=O)O17.01-1:C*C*C*C*C*C*11.71-C(=O)O-4.3generalcorrectionsCH340.6-2.3aliphatic28.31alpha-N9.31beta-1:C*C*C*C*C*C*19.41beta-C0.31delta-C-4.4generalcorrectionsCH340.6-2.3aliphatic28.31alpha-N9.31beta-1:C*C*C*C*C*C*19.41beta-C0.31delta-C-4.4generalcorrectionsCH125.2126.72-thiophene1.11-C(=O)O-3.91-1:C*C*C*C*C*C*11.31-C(=O)OC133.5126.72-thiophene6.81-C(=O)O0.81-1:C*C*C*C*C*C*17.41-C(=O)O-8.2generalcorrectionsC128.7125.62-thiophene9.11-C(=O)O-0.31-1:C*C*C*C*C*C*18.31-C(=O)O-14.0generalcorrectionsCH316.1-2.3aliphatic24.31alpha-1:C*C*C*C*C*C*1-5.11gamma-N0.31delta-1:C-S-C=C-C=10.62delta-C-1.7generalcorrectionsC162.6166.01-carboxyl0.01-1:C-S-C=C-C=1-3.4generalcorrectionsC163.4166.01-carboxyl0.01-1:C=C-S-C=C-1-2.6generalcorrections
本文标题:2016级硕士生计算机在化学与材料科学中的应用试题
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