Reversible Addition of Olefins and Other Molecules to Heavier Main group Molecules and Related Reactions
烯烃和其他分子向较重主族分子的可逆加成及相关反应
基本信息
- 批准号:0948417
- 负责人:
- 金额:$ 52.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Continuing Grant
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-02-01 至 2014-01-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
This award in the Chemical Synthesis (SYN) program supports work by Professor Philip P. Power at the University of California, Davis to carry out fundamental studies on the reversible reactions of unsaturated molecules with multiple bonded heavier main group and transition metal species. These studies focus on how small molecules containing multiple bonds interact in reversible processes with a group of elements that have not been well studied up to now. Examples of the small unsaturated (that is, multiple bonded) molecules to be studied include ethylenes, acetylenes, carbon monoxide and carbon dioxide. These molecules are of great importance in industrial catalytic cycles which usually use transition metal compounds of metals such as titanium, rhodium or platinum as catalysts.The studies will focus on abundant and inexpensive elements such as aluminum or silicon whose use may achieve better catalysis together with energy savings. In addition, the award supports the training of several undergraduate and graduate students and postdoctoral fellows in numerous practical research skills as well as in independent scientific thinking.
化学合成(SYN)计划中的这一奖项支持加州大学戴维斯分校的Philip P. Power教授的工作,对具有多个键合的较重主基和过渡金属物种的不饱和分子的可逆反应进行基础研究。这些研究的重点是如何包含多个键的小分子在可逆过程中与一组尚未得到很好研究的元素相互作用。要研究的不饱和(即多重键合)小分子的例子包括乙烯、乙炔、一氧化碳和二氧化碳。这些分子在工业催化循环中非常重要,通常使用金属如钛、铑或铂的过渡金属化合物作为催化剂。研究将集中在丰富和廉价的元素如铝或硅,它们的使用可以实现更好的催化和节能。此外,该奖项还支持多名本科生和研究生以及博士后研究员在众多实践研究技能以及独立科学思维方面的培训。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Philip Power其他文献
Philip Power的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Philip Power', 18)}}的其他基金
Using London Dispersion Force Effects to Stabilize Inorganic and Organometallic Molecules
利用伦敦色散力效应稳定无机和有机金属分子
- 批准号:
2152760 - 财政年份:2022
- 资助金额:
$ 52.5万 - 项目类别:
Standard Grant
Designing Enhanced Dispersion Force Effects Into Inorganic and Organometallic Molecules
设计无机和有机金属分子的增强色散力效应
- 批准号:
1565501 - 财政年份:2016
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Synthesis and Characterization of Transition Metal and Main Group Complexes with Unusual Bonding and Physical Properties
具有异常键合和物理性质的过渡金属和主族配合物的合成与表征
- 批准号:
1263760 - 财政年份:2013
- 资助金额:
$ 52.5万 - 项目类别:
Standard Grant
The Singlet Diradical Character of Multiple Bonded Compounds of the Heavier Group 13 and 14 Elements
重13族和14族元素多重键合化合物的单线态双自由基特征
- 批准号:
0641020 - 财政年份:2007
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Sterically and Electronically Modified Terphenyl Ligands in Main Group Chemistry
主族化学中的空间和电子修饰的三联苯配体
- 批准号:
0346715 - 财政年份:2004
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Synthesis and Characterization of New Molecular Clusters of Tetrels
Tetrels新分子簇的合成与表征
- 批准号:
0304871 - 财政年份:2003
- 资助金额:
$ 52.5万 - 项目类别:
Standard Grant
New Low Valent Group 13, 14 and 15 Species Stabilized by Ligands with Flanking Aryl Groups
由侧翼芳基配体稳定的新低价族 13、14 和 15 物种
- 批准号:
0094913 - 财政年份:2001
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Higher-order Homo and Heteronuclear Multiple Bonding Involving Main Group Elements
涉及主族元素的高阶同质和异核多重键合
- 批准号:
9730099 - 财政年份:1998
- 资助金额:
$ 52.5万 - 项目类别:
Standard Grant
Element-Element and Related Bonding in the Earlier Main Group Elements
早期主族元素中的元素-元素及相关键合
- 批准号:
9422494 - 财政年份:1995
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Synthesis and Structural Characterization of Novel Main Group Compounds with Multiple Bonding
新型多重键合主族化合物的合成及结构表征
- 批准号:
9121065 - 财政年份:1992
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
相似海外基金
Asymmetric Pd-Catalyzed Conjugate Addition of Boronic Acids to Acceptor-Substituted Olefins - An Enantioselective Access to All-Carbon Quaternary Stereocenters
钯不对称催化硼酸与受体取代的烯烃的共轭加成——对映选择性获得全碳四元立构中心
- 批准号:
217049976 - 财政年份:2012
- 资助金额:
$ 52.5万 - 项目类别:
Research Fellowships
catalytic Asmmetric Oxy- and Azido-1,4-Addition to Activated Olefins
活性烯烃的催化不对称氧加成和叠氮基 1,4-加成
- 批准号:
358338-2008 - 财政年份:2009
- 资助金额:
$ 52.5万 - 项目类别:
Postdoctoral Fellowships
catalytic Asmmetric Oxy- and Azido-1,4-Addition to Activated Olefins
活性烯烃的催化不对称氧加成和叠氮基 1,4-加成
- 批准号:
358338-2008 - 财政年份:2008
- 资助金额:
$ 52.5万 - 项目类别:
Postdoctoral Fellowships
Catalytic Addition of Nucleophiles to Unactivated Olefins
亲核试剂与未活化烯烃的催化加成
- 批准号:
0555425 - 财政年份:2006
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Kinetic isotope effects as probes for glycoside transition state structure characterisation of reactive intermediates, formed during electrophilic addition to olefins
动力学同位素效应作为探针,用于表征在烯烃亲电加成过程中形成的反应中间体的糖苷过渡态结构
- 批准号:
121348-1992 - 财政年份:1993
- 资助金额:
$ 52.5万 - 项目类别:
Discovery Grants Program - Individual
Kinetic isotope effects as probes for glycoside transition state structure characterisation of reactive intermediates, formed during electrophilic addition to olefins
动力学同位素效应作为探针,用于表征在烯烃亲电加成过程中形成的反应中间体的糖苷过渡态结构
- 批准号:
121348-1992 - 财政年份:1992
- 资助金额:
$ 52.5万 - 项目类别:
Discovery Grants Program - Individual
Elementary Steps in the Nucleophilic Addition to Olefins
烯烃亲核加成的基本步骤
- 批准号:
8024261 - 财政年份:1981
- 资助金额:
$ 52.5万 - 项目类别:
Continuing Grant
Mechanisms of Electrophilic Addition Reactions of Olefins
烯烃亲电加成反应机理
- 批准号:
8022783 - 财政年份:1981
- 资助金额:
$ 52.5万 - 项目类别:
Continuing grant
Kinetics and Mechanism of Addition of Acids to Olefins
酸与烯烃加成的动力学和机理
- 批准号:
66P5103 - 财政年份:1966
- 资助金额:
$ 52.5万 - 项目类别: