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光激活烯烃复分解:催化剂开发、合成及应用。

Light-Activated Olefin Metathesis: Catalyst Development, Synthesis, and Applications.

机构信息

Department of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.

Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.

出版信息

Acc Chem Res. 2020 Oct 20;53(10):2456-2471. doi: 10.1021/acs.accounts.0c00495. Epub 2020 Sep 29.

Abstract

The most important means for tuning and improving a catalyst's properties is the delicate exchange of the ligand shell around the central metal atom. Perhaps for no other organometallic-catalyzed reaction is this statement more valid than for ruthenium-based olefin metathesis. Indeed, even the simple exchange of an oxygen atom for a sulfur atom in a chelated ruthenium benzylidene about a decade ago resulted in the development of extremely stable, photoactive catalysts. This Account presents our perspective on the development of dormant olefin metathesis catalysts that can be activated by external stimuli and, more specifically, the use of light as an attractive inducing agent.The insight gained from a deeper understanding of the properties of -dichlororuthenium benzylidenes opened the doorway for the systematic development of new and efficient light-activated olefin metathesis catalysts and catalytic chromatic-orthogonal synthetic schemes. Following this, ways to disrupt the ligand-to-metal bond to accelerate the isomerization process that produced the active precatalyst were actively pursued. Thus, we summarize herein the original thermal activation experiments and how they brought about the discoveries of photoactivation in the sulfur-chelated benzylidene family of catalysts. The specific wavelengths of light that were used to dissociate the sulfur-ruthenium bond allowed us to develop noncommutative catalytic chromatic-orthogonal processes and to combine other photochemical reactions with photoinduced olefin metathesis, including using external light-absorbing molecules as "sunscreens" to achieve novel selectivities. Alteration of the ligand sphere, including modifications of the N-heterocyclic carbene (NHC) ligand and the introduction of cyclic alkyl amino carbene (CAAC) ligands, produced more efficient light-induced activity and special chemical selectivity. The use of electron-rich sulfoxides and, more prominently, phosphites as the agents that induce latency widened the spectrum of light-induced olefin metathesis reactions even further by expanding the colors of light that may now be used to activate the catalysts, which can be used in applications such as stereolithography and 3D printing of tough metathesis-derived polymers.

摘要

调变和改善催化剂性能的最重要手段是精细交换中心金属原子周围的配体壳。对于钌基烯烃复分解反应来说,这句话可能比其他任何有机金属催化反应都更有意义。事实上,就在大约十年前,在螯合的钌亚苄基中简单地将一个氧原子交换为一个硫原子,就导致了极其稳定的、有光活性的催化剂的发展。本综述介绍了我们对开发可被外部刺激激活的休眠烯烃复分解催化剂的看法,更具体地说,是使用光作为有吸引力的诱导剂。从对二氯合钌亚苄基性质的更深入理解中获得的见解,为系统开发新的和有效的光激活烯烃复分解催化剂以及催化变色正交合成方案打开了大门。在此之后,人们积极探索破坏配体-金属键以加速产生活性前催化剂的异构化过程的方法。因此,我们总结了本文中原始的热激活实验,以及它们如何带来硫螯合亚苄基催化剂家族中光激活的发现。用于解离硫-钌键的特定波长的光使我们能够开发非交换催化变色正交过程,并将其他光化学反应与光诱导烯烃复分解相结合,包括使用外部光吸收分子作为“防晒霜”以实现新的选择性。配体球的改变,包括 N-杂环卡宾(NHC)配体的修饰和环状烷基氨基卡宾(CAAC)配体的引入,产生了更有效的光诱导活性和特殊的化学选择性。富电子亚砜的使用,更突出的是膦酸酯,作为诱导潜伏的试剂,通过扩展现在可用于激活催化剂的光的颜色,进一步拓宽了光诱导烯烃复分解反应的范围,这些催化剂可用于立体光刻和坚韧的复分解衍生聚合物的 3D 打印等应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b40/7584343/3d97cd25ec90/ar0c00495_0020.jpg

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