CAS: Collaborative Research: Electronic Structure/Function Relationships Underpinning Atom Transfer Reactivity
CAS:合作研究:支撑原子转移反应性的电子结构/功能关系
基本信息
- 批准号:2247817
- 负责人:
- 金额:$ 36.1万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-07-15 至 2026-06-30
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
With the support of the Chemical Structure, Dynamics & Mechanisms-B Program of the Chemistry Division, Professors Theodore Betley of the Department of Chemistry and Chemical Biology at Harvard University and Kyle Lancaster of the Department of Chemistry and Chemical Biology at Cornell are investigating the electronic structure of radicaloid ligand transition metal complexes. This collaborative project seeks to synthesize and characterize novel metal-ligand multiple bond (MLMB) systems that can deliver diverse functionalities into carbon hydrogen bond substrates. The ability to selectively incorporate functionality into unactivated carbon hydrogen bonds represents a significant advance in converting inexpensive chemical feedstocks (e.g. hydrocarbons) to value-added molecules (e.g., pharmaceutical precursors). The joint project will leverage the combined expertise of the Lancaster group to perform inorganic spectroscopy and the Betley group’s expertise in synthesis to explore periodic trends in the electronic structure and reactivity of mono- and trinuclear transition metal complexes bearing nitrenoid and nitrido ligands. The project lies at the interface of inorganic and organometallic chemistry and is therefore well suited to the education of scientists at all levels. These groups organize and participate in interactive demonstrations for students at the K-12 level from local grade schools and high schools. Here the students are invited to participate in a series of experiments and observe chemical phenomena at their laboratories. The overarching goals of the project are to probe how metal-ligand compositions and their changing oxidation levels alter the resultant physical properties and reactivity for these coordination complexes. To this end, they seek to synthesize mono- and trinuclear complexes featuring nitrenoid and nitrido functionalities to examine and harness their reaction chemistry. Thus, they aim to address the following questions: (1) How are molecular redox processes distributed along the primary redox pair in MLMB associations? (2) How do molecular redox changes of MLMBs alter oxidative group transfer processes? (3) For cluster-bound imido/nitrido complexes, how is the redox load localized? (4) For cluster-bound functionalities, can ligand hole character accumulate under oxidative processes? The target open-shell units will be designed to support a breadth of molecular oxidation states, altering the electronic structure of the MLMB or cooperatively bound moiety. They will leverage N K-edge XAS as means to probe the sub-octet character of coordinated N-donors and to quantify M–N covalency in coordination complexes. These data will be used to rationalize periodic trends in the reactivity (nucleophilic vs. electrophilic) of MLMB and cluster-based complexes across the late first transition series.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
在化学系化学结构、动力学和机理b项目的支持下,哈佛大学化学和化学生物学系的Theodore Betley教授和康奈尔大学化学和化学生物学系的Kyle Lancaster教授正在研究自由基配体过渡金属配合物的电子结构。该合作项目旨在合成和表征新型金属配体多键(MLMB)系统,该系统可以将多种功能传递到碳氢键底物中。选择性地将功能结合到非活性碳氢键中的能力代表了将廉价化学原料(例如碳氢化合物)转化为增值分子(例如,药物前体)的重大进步。该联合项目将利用兰开斯特集团在无机光谱方面的综合专业知识和Betley集团在合成方面的专业知识,探索含有类氮和氮配体的单核和三核过渡金属配合物的电子结构和反应性的周期性趋势。该项目处于无机化学和有机金属化学的交叉点,因此非常适合各级科学家的教育。这些团体为当地小学和高中的K-12年级学生组织并参与互动示范。在这里,学生们被邀请参加一系列的实验,并在他们的实验室观察化学现象。该项目的总体目标是探索金属配体组成及其氧化水平的变化如何改变这些配位配合物的最终物理性质和反应性。为此,他们寻求合成具有类氮和氮功能的单核和三核配合物,以研究和利用它们的反应化学。因此,他们的目标是解决以下问题:(1)在MLMB关联中,分子氧化还原过程是如何沿着主要氧化还原对分布的?(2) mlmb分子氧化还原变化如何改变氧化基转移过程?(3)对于簇结合的亚胺/氮杂络合物,氧化还原负荷是如何定位的?(4)对于团簇结合官能团,配体空穴特征是否会在氧化过程中积累?目标开壳单元将被设计成支持分子氧化态的宽度,改变MLMB或协同结合片段的电子结构。他们将利用N- k边XAS作为手段来探测配位N给体的亚八元体特征,并量化配位配合物中的M-N共价。这些数据将用于理顺MLMB和簇基配合物的反应性(亲核与亲电)的周期性趋势。该奖项反映了美国国家科学基金会的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
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)
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Theodore Betley其他文献
Theodore Betley的其他文献
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{{ truncateString('Theodore Betley', 18)}}的其他基金
MRI: Acquisition of Single-Crystal Diffractometer for Small Molecule Crystallography and Cryosystem
MRI:获取用于小分子晶体学和冷冻系统的单晶衍射仪
- 批准号:
2216066 - 财政年份:2022
- 资助金额:
$ 36.1万 - 项目类别:
Standard Grant
CAS: Collaborative Research: Electronic Structure/Function Relationships in Base Metal Complexes Spanning the Oxo/Oxene and Imide/Nitrene Continuum
CAS:合作研究:跨越氧代/氧烯和酰亚胺/氮烯连续体的贱金属配合物中的电子结构/功能关系
- 批准号:
1954690 - 财政年份:2020
- 资助金额:
$ 36.1万 - 项目类别:
Standard Grant
CAREER: Iron mediated catalytic C-H bond functionalization
职业:铁介导的催化 C-H 键功能化
- 批准号:
0955885 - 财政年份:2010
- 资助金额:
$ 36.1万 - 项目类别:
Continuing Grant
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