In this paper, a "two-molecule" model of ellipsoidal drop was established.And then the ellipsoid situation was transformed into sphere situation by coordinate transformation.By utilizing bipolar coordinates and Maxwell stress tensor, the expression of electrostatic radial and tangential forces between two drops was deduced.

通過建立水滴的"二分子"橢球模型，利用坐標變換把橢球問題轉換成圓球問題，并運用雙球面坐標和Maxwell應力張量理論，推導出兩橢球水滴間的徑向和切向電場力的表達式色综合色综合色综合免费视频。

They had suppressed the cathodic process of carbon steel electrode. Their inhibition performance was also related with their molecule stereo conformation and electron configuration. Four of bis-(1, 1'-benzotriazoly)-α,β-diamide compounds linked via-CO 〓CO-chain were synthesized and certified by IR and 〓H-NMR. The minimum energy conformations of these compounds were obtained by MM2 forcefield program. The two benzotriazole moiety in BBT1 was more planar than in other compounds. This was beneficial in increasing the inhibition effects of BBT1. In 0.5M H〓SO〓 solution, BBT1 suppressed anodic corrosion reaction. In 3%NaCl solution, BBT1 suppressed both cathodic and anodic corrosion reactions. 1- [ (1'-imidazolly)-methyl] benzotriazole was synthesized by Mannich reaction.

合成了四個通過-CO〓CO-連接的雙（1，1'-苯并三唑）-α日日干人人干，ω-二酰胺化合物一级免费黄片，采用MM2分子力學程序優(yōu)化了它們的分子結構，雙（1中文字幕最新，1'-苯并三唑）-α中文字幕欧美，ω-二酰胺化合物的緩蝕作用與其分子內兩個苯并三唑單元的空間取向有關系，良好的平面性有利于苯并三唑二聚體的吸附和緩蝕作用在线亚洲欧美专区国产，苯并三唑二聚體BBT1分子內兩個苯并三唑單元近似平行操我国产，所以顯示出較好的緩蝕效果。0.5M硫酸中BBT1主要抑制銅的陽極溶解的電化學反應男人爽插女人的网站在线看；3％NaCl溶液中国产美女裸体一区二区三区久久久体验视频，BBT1對銅的陽極溶解和氧的陰極還原過程均有抑制作用，相比較而言對陰極過程的抑制作用更大一些几岁小孩啪啪啪黄色视频。

The preliminary stiochiometric analysis showed that when the enzyme metabolized EDDA, two acetyl groups were removed and ethylenediamine and two glyoxylates were produced in the presence of oxygen.

然后對該酶促反應進行了定量分析：結果顯示在IDA氧化酶的作用下每代謝一分子的EDDA將生成二分子的乙醛酸及一分子的乙二胺久久精品这里热有精品6，同時也檢測到過氧化氫的生成。

The conclusions were as follows: theνO-H andνC=O IR absorption maxima shifted towards higher wave numbers after imprinting 17β-estradiol on TFMAA-co-TRIM copolymer with the red shift of theνO-H groups being apparent after precipitation polymerization for 16h while that forνC=O groups being observed after polymerization for 24h. A strong interaction between TFMAA and 17β-estradiol was confirmed by the high selectivity for 17β-estradiol, as indicted by the values of the separation factor of isomers of 17β-estradiol/17α-estradiol (2.28) and the imprinted factor (3.01). Particle diameter of TFMAA-co-TRIM polymer was between 300 nm and 1.5μm, which suited well for solid phase sorbent throughout at low column pressure. The recognition of imprinting TFMAA-co-TRIM polymer for sterol molecules was driven by enthalpy eluted with acetronitile, and low temperature was in favor of the separation of sterol structure analogues on imprinting column. TFMAA-co-TRIM polymer possessed of determinate anti-heat stability, with melting point beginning at 255.84℃, Tp=257.40℃, control TFMAA-co-TRIM polymer and imprinting TFMAA-co-TRIM polymer were respectively decompounded at 267.79℃and 343.11℃, and solid micro-extraction noddle prepared by the special polymerization also showed definite recognition for 17β-estradiol by GC/MS detecting at 270℃. By selection of various washing and elution solvents, elution reagents of close polymerization system were of more advantage in template molecules retention and recognition on molecularly imprinted solid phase extraction column. At a certain extent, progesterone, 17α-estradiol, 17β-estradiol and 4-androstene-3, 17-dione could be intercepted on the MISPE column. Especially, MISPE had high selectivity for progesterone, and imprinting TFMAA-co-TRIM polymer could achieve adsorption balance within 50 min by absorption kinetics test for 17β-estradiol. However, MISPE column showed better selectivity and enrichment property for 17β-estradiol than C18 and CSPE columns according to the data from HPLC and GC/MS analyses. Recovery of 17β-estradiol on MISPE column was up to 85.5% while when prime extracting solution of milk powder was sampled, the recovery of CSPE and C18 columns were 43.7% and 30.7%, respectively.

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In this thesis,the AM1,MNDO,MINDO/3(mainly AM1)and INDO/S-CI semiempirical MO methods were used toinvestigate the excited-state intramolecular protontransfer reactions of salicylic acid derivatives—salicylic acid,methyl salicylate,salicylaldehyde,o-hydroxyaceto-phenone,salicylamide and 3-hydroxy-picolinamide (6 conformers and 2-3 anion species);2-(2'-hydroxy-5' methylphenyl) benzotriazole(4 conformers),2-(2' hydroxyphenyl) benzimidazole (3 conformers and 3anion species),Bis-2,5-(2-benzoxazolyl)hydroquinone(3 conformers),2-(2'-hydroxyphenyl)benzothiazole(2conformers) and 7-azaindole dimer (2 conformers).Theinvestigations were described as follows.Geometry optimization,relative stability andhydrogen bonding energy First,for sylicylic acid derivative molecules,the AM1,MNDO and MINDO/3 methods were used toinvestigate ground-state geometry optimization,energies,relative stabilities and hydrogen-bondingenergies on the five kinds of the molecules(designing 6 conformers and 2-3 anion species).Comparing with experimental data,the optimizedgeometry,the order of stability,the hydrogen-bonding energies and the distances between O-O in O-H..O hydrogen bonds by AM1 method were in agreementwith the experimental data,however,the C-C bondlengths optimized by MNDO and MINDO/3 were longer,C-O and O-H bond lengths were shorter;for C-N bondlengths,the results opitimized by MNDO method werethe same as those by AM1 method,nevertheless the C-Nbond lengths given by MINDO/3 method were muchshorter.For some sylicylic acid derivatives(e.g.methyl salicylate,salicylamide),the order ofstabilities on the conformers given by MNDO andMINDO/3 methods were not in agreement with theexisting conformers deduced by experimental methods,and the hydrogen bonding energies calculated by MNDO.and MINDO/3 methods were smaller.Second,the studyon the other systems found that the optimizedgeometry of the proton-transfered product with INDOmethod could not be obtained,only could theoptimized geometry of reactant be obtained,and thecalculated hydrogen bonding energies were greater.Many results of calculation indicated that the studyon the excited-state intramolecular proton transferreaction system using AM1 method was suitable andreliable.

本論文用AM1免费精品国产高清在线观看、MNDO、MINDO/3（主要是AM1）和INDO/S-CI半經驗分子軌道方法對水楊酸衍生物系列——水楊酸自拍美日韩在线视频网站免费、水楊酸甲酯手机在线看永久AV片免费无毒、水楊醛、O-羥基乙酰苯酮欧美日韩在线视、水楊酰胺和3-羥基吡啶酰胺（6種異構體和2-3種陰離子）精品推荐本地黄色视频；2-（2'-羥基-5'-甲基苯基）苯并三〓唑（4種異構體）；2-（2'-羥基苯基）苯并咪唑（3種異構體和3種陰離子）欧美老年性生活视频；2在线播放你懂的网站，5-二間氮雜氧茚氫醌（3種異構體）；2-（2'-羥基苯基）間〓雜硫茚（2種異構體）和7-〓吲哚二體（2種異構體）的激發(fā)態(tài)分子內質子轉移反應在以下幾個方面進行了較系統(tǒng)的理論研究：幾何構型優(yōu)化和相對穩(wěn)定性及氫鍵能首先以水楊酸衍生物系列分子為例A片免费观看久，用AM1国产a√视色、MNDO和MINDO/3方法考察了5種分子（每種分子設計6種異構體和2-3種陰離子）的基態(tài)幾何構型優(yōu)化，能量思思玖玖、相對穩(wěn)定性和氫鍵能計算www簧片网址视频，通過和實驗數(shù)據(jù)進行比較，AM1方法給出的優(yōu)化幾何構型亚洲人成网网址在线看、穩(wěn)定性次序日韩AAAAAA免费毛片、氫鍵能和O—H。无码国内精品麻豆久久人妻。日本特级黄色大片天天高潮免费看。O氫鍵的0—0距離與實驗數(shù)據(jù)吻合最好，MNDO和MINDO/3方法優(yōu)化的C-C鍵長偏長日本黄色视频网址，C-O鍵和O-H鍵長偏短欧美草草操在线视频；對于C-N鍵長，MNDO和AM1優(yōu)化結果差別不大色久是色，而MINDO/3給出了過短的C-N鍵長www又湿又大，MNDO和MINDO/3方法給出的有些水楊酸衍生物分子（如水楊酸甲酯和水楊酰胺）異構體的穩(wěn)定性次序和實驗上推測的可存在異構體結果不一致，MNDO和MINDO/3方法給出的氫鍵能偏低一本二本三本黄色视频，對其他體系的研究發(fā)現(xiàn)INDO方法常常不能得到質子轉移產物的優(yōu)化幾何構型怡红院最新地址，只能得到反應物的優(yōu)化構型久久视频一二区，并且估算的氫鍵能偏高，大量的計算結果表明AM1方法對本論文研究的激發(fā)態(tài)分子內質子轉移反應體系是適宜和可靠的69视频在线免费看。

A diacid triglyceride containing two molecules of palmitic acid and one of stearic acid could be named dipalmitostearin or steartodipalmtin.

含有二分子棕櫚酸和一分子硬脂酸的二酸式甘油三酸脂可命名為二棕櫚酰硬脂酰甘油酯或硬脂酰二棕櫚酰甘油酯国产欧美精品亚洲AMV。

A diacid triglyceride containing two molecules of palmiticacid and one of stearic acid could be named dipalmitostearin orsteartodipalmtin.

含有二分子棕櫚酸和一分子硬脂酸的二酸式甘油三酸脂可命名為二棕櫚酰硬脂酰甘油酯或硬脂酰二棕櫚酰甘油酯。

In this thesis, a series of complexes based on aromatic multicarboxylic acids have been successfully synthesized in solutions or under hydrothermal conditions. Their structure and properties are investigated.(1) Eight complex compounds have been synthesized and characterized by X-ray single crystal diffractive technology: The eight complexes are listed as following: [Cu242] complex 1 [Cd22(H2O)4]·4H2O complex 2 [Co(H2btc)(H2O)3] complex 3 [Co2(H2O)2]·H2O complex 4 [Ni22(H2O)4] complex 5 [Cu22(H2O)4] complex 6 [Co(H2biim)2(H2O)2](H2btc) complex 7 [Zn(H2biim)2(H2O)2](H2btc) complex 8 The structure of complex 1 is dinuclear complex resulted from weak interactions（0-D chain）; complex 2 is 1-D chain stucture result from interactions of water molecules; complex 3动漫无码av永久免费专区、4人人插人人爽爽人人干射、5、6 are coordination polymers using hydrothermal synthses, where the first kind ligand is H4btc, the second kind ligand is phen and Co2+欧美黄色网站免费的、Ni2+午夜福利小黄片、Cu2+ as center ions, respectively. While the coordination enviroment of Co2+ is the same in complex 3, the coordination geometries around the Co atoms in complex 4 are obviously different because of the different reaction conditions. In complex 4, the 1-D chains are connected into 2-D layer through carboxy groups of ligand H4btc. The structures of complex 5、6 are 1-D chain stucture result from interactions of carboxy groups in ligand H4btc. Complex 7狼友免费观看不卡网站、8 are homeomorphy compounds. Either of them are linked to the 3-D chains through intermolecular hydrogen bonds. Each H4btc lose two protons and H2btc2- acts as negative electron balance.

合成了8個結構新穎的配合物a亚洲A片视频网，并用X-射線單晶結構分析方法確定了晶體結構，分別為： [Cu242] 配合物1 [Cd22(H2O)4]·4H2O 配合物2 [Co(H2btc)(H2O)3] 配合物3 [Co2(H2O)2]·H2O 配合物4 [Ni22(H2O)4] 配合物5 [Cu22(H2O)4] 配合物6 [Co(H2biim)2(H2O)2](H2btc)配合物7 [Zn(H2biim)2(H2O)2](H2btc)配合物8 配合物1是一個依靠弱作用連接的雙核銅結構最新的毛片网址；配合物2借助水分子形成一維鏈狀結構一级a做片免费看欧美一；配合物3、491自拍最新地址、5免费Jizz国产精品网站、6是以H4btc為第一配體、phen為第二配體国产一级毛片国产一级A片，通過水熱法合成的配合物番茄社区android下载，其中，Co2+AVwww网站在线、Ni2+婷婷深爱99精品五月在线视频、Cu2+為中心離子；配合物3中的二價鈷離子具有相同的配位環(huán)境国产AV黄色，不同反應條件下得到的配合物4中的二價鈷離子存在不同的配位環(huán)境一级A片C视频，在配合物4中，一維鏈通過H4btc上的羧基形成一個二維層結構国产高清色色；配合物5、6是借助H4btc上的羧基形成的一維鏈狀結構精品国产玩哟在线观看；配合物7wwwcom亚洲97、8屬于異質同晶結構，它們的分子通過分子間氫鍵形成三維網(wǎng)狀結構经典自拍视频欧美日韩在线观看，H4btc上的羧基失去2個質子少妇人妻无码免费视频，作為一個二價負離子起到電荷平衡作用。

Under different initial total egg white lysozyme concentrations in urea solution, the refolding egg white lysozyme intermediates could be deduced to have a tendency to form a bimolecular intermediate aggregate, and this inference was further confirmed by their nonreducing SDS-PAGE and size exclusion chromatography.

當不同濃度蛋白溶菌酶在脲溶液中復性時精品国产福利在线观看，蛋白溶菌酶折疊中間體有形成二分子積聚體的趨勢淫荡的欧美性爱视频，這個推測得到了非還原電泳和體積排阻色譜結果的證實亚洲欧美国产日韩综合久久。

By using lysozyme as model protein, this equation was tested with the renaturation process of three kinds of denatured lysozyme molecules in urea and guanidine hydrochloride solutions, and it was found that the renaturation results of denatured lysozymes could be described well by this equation, and these denatured lysozyme molecules had a tendency to form a bi-molecular intermediate aggregate in both solutions.

以三種溶菌酶在脲和鹽酸胍溶液中的變性-復性過程對此方程進行了驗證，結果表明所給出的方程能夠很好地描述三種溶菌酶在這兩種變性液中的復性結果欧美黑B，三種溶菌酶在兩種變性液中有形成二分子集聚體的趨勢国产一级毛片黑白配。

dyad, diad：二價染色體;二分子

dwellings of early man 早期人類棲所 | dyad; diad 二價染色體;二分子 | dyes 染料

diatomic molecule：二原子分子,雙原子分子

diatomic excimer 二原子準分子 | diatomic molecule 二原子分子,雙原子分子 | diatomic molecules gas laser 二原子氣體激光器

diglyceride：二甘油化合物;二甘油脂

二分子;二子 diad | 二甘油化合物;二甘油脂 diglyceride | 二果瓣的 dicarpellous

oxalic acid：草酸;乙二酸

名稱: 草酸,乙二酸(Oxalic Acid) 分子式: C2H2O4 CAS編號: 144-62-7 RTECS編號: RO2450000 技術標準: GB1626-88 產品性態(tài): 草酸一般含有二分子結晶水,為白色晶體,其晶體結構有α型和β型兩種形態(tài),熔點分別為189.5℃和182℃,

oxalic acid：乙二酸

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bimolecular reaction：二分子反應

bimolecular nucleophilic substitution 雙分子親核取代<作用> | bimolecular reaction 二分子反應 | bin system 倉儲系統(tǒng)

dimolecular：雙分子

dimolecular 二分子的 | dimolecular 雙分子 | dimorphicdimorphous 同種二形的

dimolecular：二分子的

dimolecular 二分子 | dimolecular 二分子的 | dimolecular 雙分子

dimolecular：二分子

dimnessduskiness 微暗 | dimolecular 二分子 | dimolecular 二分子的

dimolecular：雙分子 二分子 二分子的

dimness 暗淡 | dimolecular 雙分子 二分子 二分子的 | dimonoecious 同株二型花