Synthesis, Structures, and Reactivity of Single and Double Cyclometalated Complexes Formed by Reactions of [Cp*MCl] (M = Ir and Rh) with Dinaphthyl Phosphines.

Clicks: 309
ID: 23763
2018
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Steady

Ranked #128 of 475 articles by views in ACS omega

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 475 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Reactions of two dinaphthyl phosphines with [Cp*IrCl] have been carried out. In the case of di(α-naphthyl)phenylphosphine (), a simple P-coordinated neutral adduct is obtained. However, -butyldi(α-naphthyl)phenylphosphine () is cyclometalated to form [Cp*IrCl(P^C)] (). Complexes and undergo further cyclometalation to give the corresponding double cyclometalated complexes [Cp*Ir(C^P^C)] (,) upon heating. In the presence of sodium acetate, reactions of , with [Cp*IrCl] directly afford the final double cyclometalated complexes (,). In the absence of acetate, [Cp*RhCl] shows no reaction with ,, whereas with acetate the reactions form the corresponding single cyclometalated complexes [Cp*RhCl(P^C)] (,), which react with BuOK to form the corresponding rhodium hydride complexes (,). Treatment of with CuCl or I leads to opening of two Ir-C σ bonds to yield the corresponding P-coordinated iridium dihalide ( or ) by means of an intramolecular C-C coupling reaction. A new chiral phosphine () is formed by the ligand-exchange reaction of with PMe. Reactions of the single cycloiridated complex with terminal aromatic alkynes result in the corresponding five- and six-membered doubly cycloiridated complex and/or η-alkene coordinated complexes ; the latter discloses that the electronic effect of terminal alkynes affects the regioselectivity. While the single cyclorhodated complex reacts with terminal aromatic alkynes to form the corresponding six-membered cyclometalated complexes by vinylidene rearrangement/1,1-insertion. Plausible pathways for formation of insertion products were proposed. Molecular structures of twelve new complexes were determined by X-ray diffraction.
Reference Key
zhang2018synthesisacs Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Zhang, Shaowei;Chu, Xiaodan;Li, Tongyu;Wang, Zhuo;Zhu, Bolin;
Journal ACS omega
Year 2018
DOI
10.1021/acsomega.8b00193
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.