系列次序

词组短语

series order

与系列次序相关的网络例句 [注：此内容来源于网络，仅供参考]

These dendritic NOBIN derived Schiff base ligands have been applied to titanium catalyzed hetero-Diels-Alder reaction of Danishefshy's diene and aldehydes, affording the corresponding 2-substituted 2, 3-dihydro-4H-pyran-4-one in quantitative yields and excellent enantioselectivities (up to 97. 2%ee). Comparing the reactivities and enantioselectivities of reaction catalyzed by the titanium complexes of these Schiff base ligands, it was found that a series of ligands L〓 were superior to the other three series of ligands L〓, L〓 and L〓, a significant positive NLE and a dendrimer effect existed in the L〓 dendritic catalyst system. The disposition of the dendritic wedges and the dendron size in the ligands were observed to have a significant impact on the enantioselectivity of the reaction.

NOBIN衍生的树枝状大分子希夫碱手性配体与钛形成的配合物在催化不对称杂Diels-Alder反应中的应用将得到的四个系列NOBIN衍生的树枝状希夫碱三齿手性配体与四异丙氧基钛形成的配合物用于催化Danishefsky's diene与醛的不对称杂Diels-Alder反应，通过反应条件的优化，获得了定量的收率和最高达97.2％ee值的对映选择性；考察了这四个系列NOBIN衍生的树枝状希夫碱钛配合物的催化活性和对映选择性，结果发现它们的活性次序依次为L〓≈L〓＞L〓＞L〓，对映选择性次序依次为L〓＞L〓＞L〓＞L〓。

Requires five series of values in this order

所需的五项数据系列必须按该次序排列

The participant manner and the interferential mechanism of the adscititious reagents are different each other.

归纳得到系列Me〓参与形成药物-BSA-Me〓复合物的稳定性、药物对BSA内源荧光的猝灭效应等作用参数按照Me〓种类的排列次序。

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.

本论文用AM1、MNDO、MINDO/3（主要是AM1）和INDO/S-CI半经验分子轨道方法对水杨酸衍生物系列——水杨酸、水杨酸甲酯、水杨醛、O-羟基乙酰苯酮、水杨酰胺和3-羟基吡啶酰胺（6种异构体和2-3种阴离子）；2-（2'-羟基-5'-甲基苯基）苯并三〓唑（4种异构体）；2-（2'-羟基苯基）苯并咪唑（3种异构体和3种阴离子）；2，5-二间氮杂氧茚氢醌（3种异构体）；2-（2'-羟基苯基）间〓杂硫茚（2种异构体）和7-〓吲哚二体（2种异构体）的激发态分子内质子转移反应在以下几个方面进行了较系统的理论研究：几何构型优化和相对稳定性及氢键能首先以水杨酸衍生物系列分子为例，用AM1、MNDO和MINDO/3方法考察了5种分子（每种分子设计6种异构体和2-3种阴离子）的基态几何构型优化，能量、相对稳定性和氢键能计算，通过和实验数据进行比较，AM1方法给出的优化几何构型、稳定性次序、氢键能和O—H。。。O氢键的0—0距离与实验数据吻合最好，MNDO和MINDO/3方法优化的C-C键长偏长，C-O键和O-H键长偏短；对于C-N键长，MNDO和AM1优化结果差别不大，而MINDO/3给出了过短的C-N键长，MNDO和MINDO/3方法给出的有些水杨酸衍生物分子（如水杨酸甲酯和水杨酰胺）异构体的稳定性次序和实验上推测的可存在异构体结果不一致，MNDO和MINDO/3方法给出的氢键能偏低，对其他体系的研究发现INDO方法常常不能得到质子转移产物的优化几何构型，只能得到反应物的优化构型，并且估算的氢键能偏高，大量的计算结果表明AM1方法对本论文研究的激发态分子内质子转移反应体系是适宜和可靠的。

The results indicated that BaCe0.8Ho0.2O(subscript 3-α) sinters are of single-phase structures of orthorhombic perovskite. In the temperature range of 600~1000℃, the nonstoichiometric materials (x=1.03 and 0.97) have higher conductivities in wet hydrogen and wet air and better performances of hydrogen-air fuel cells than the stoichiometric one (x=1). In this series, BaCe0.8Ho0.2O(subscript 3-α) has the highest conductivities 2.10×10^(-2Scm^(-1) in wet hydrogen, 3.46×10^(-2) Scm^(-1) in wet air, at 1000℃ and the maximum power output density 122 mWcm^(-2 at 1000℃.

结果表明，在600~1000℃温度范围内、湿润氢气和湿润空气气氛中，该系列材料的电导率随温度和钡离子含量的变化均与以该系列材料为固体电解质的氢－空气燃料电池性能随温度和钡离子含量变化的次序一致，即：非化学计量组成材料BaCe0.8Ho0.2O(下标 3-α)(x=1.03， 0.97)具有较化学计量组成材料BaCe0.8Ho0.2O(下标 3-α)(x=1)高的电导率和氢－空气燃料电池输出功率密度，其中BaCe0.8Ho0.2O(下标 3-α)有最高的电导率（1000℃时、在湿润的氢气气氛中：2.10×10^(-2)Scm^(-1)；在湿润的空气气氛中：3.46×l0^(-2)Scm^(-1)）和最大的氢－空气燃料电池输出功率密度（1000℃时：122mWcm^(-2)）。

与系列次序相关的网络解释 [注：此内容来源于网络，仅供参考]

series order：系列次序

2003series number系列序号 | 2004series order系列次序 | 2005SGML标准广义置标语言

Adjusting the Series Plot Order：调整系列次序

5.Deleing a series name 图表菜单->源数据,也可以修改SERIES formula | Adjusting the Series Plot Order 调整系列次序 | Charting a Noncontinguous Range 图表中使用多个区域

Deleing a series name：图表菜单->源数据,也可以修改

4.Changing a series name 图表菜单->源数据,也可以修改SERIES formula | 5.Deleing a series name 图表菜单->源数据,也可以修改SERIES formula | Adjusting the Series Plot Order 调整系列次序