排序方式: 共有25条查询结果,搜索用时 15 毫秒
1.
Dr. Jessica Rodriguez Dr. György Szalóki Dr. E. Daiann Sosa Carrizo Dr. Nathalie Saffon-Merceron Dr. Karinne Miqueu Dr. Didier Bourissou 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(4):1527-1531
Gold(III) π-complexes have been authenticated recently with alkenes, alkynes, and arenes. The key importance of PdII π-allyl complexes in organometallic chemistry (Tsuji–Trost reaction) prompted us to explore gold(III) π-allyl complexes, which have remained elusive so far. The (P,C)AuIII(allyl) and (methallyl) complexes 3 and 3′ were readily prepared and isolated as thermally and air-stable solids. Spectroscopic and crystallographic analyses combined with detailed DFT calculations support tight quasi-symmetric η3-coordination of the allyl moiety. The π-allyl gold(III) complexes are activated towards nucleophilic additions, as substantiated with β-diketo enolates. 相似文献
2.
《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(34):10232-10236
QM/MM calculations reveal that the nickel pincer complex in lactate racemase functions as a reversible “single‐center electrode” that accepts and donates back an electron. In this way, it catalyzes the isomerization process d ‐lactate⇌l ‐lactate through successive proton‐coupled electron‐transfer steps. 相似文献
3.
Mitsuhiro Iwasaki Yukatsu Shichibu Katsuaki Konishi 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(8):2465-2469
It is well known that alkynes act as π‐acids in the formation of complexes with metals. We found unprecedented attractive Au–π interactions in diacetylene‐modified [core+exo]‐type [Au8]4+ clusters. The 4‐phenyl‐1,3‐butadiynyl‐modified cluster has unusually short Au–Cα distances in the crystal structure, revealing the presence of attractive interactions between the coordinating C≡C moieties and the neighboring bitetrahedral Au6 core, which is further supported by IR and NMR spectra. Such weak interactions are not found in mono‐acetylene‐modified clusters, which indicates that they are specific for diacetylenic ligands. The attractive Au–π interactions are likely associated with the low energy of the π* orbital in the diacetylenic moieties, into which the valence electrons of the gold core may be back donated. The [Au8]4+ clusters show clear red‐shifts of >10 nm with respect to the corresponding mono‐acetylenic clusters in UV/Vis absorption bands, which indicates substantial electronic perturbation effects of the Au–π interactions. 相似文献
4.
5.
6.
7.
8.
9.
10.