The title compound, [FePt(CHOS)(CHP)(CHP)(CO)], , [(OC)Fe(μ-dppm)(μ-C(=O)C(CHSCHMe-4)=CCHSCHMe-4)Pt(PPh)], represents the first example of a diphosphane-bridged heterobimetallic Fe-Pt dimetalla-cyclo-pentenone complex resulting from a bimetallic activation of metal-coordinated carbonyl ligand with an inter-nal alkyne, namely 1,4-bis-(-tolyl-thio)-but-2-yne. The bridging μ-C(=O)C(CHSCHMe-4)=CCHSCHMe-4 unit (stemming from a carbon-carbon coupling reaction between CO and the triple bond of the alkyne di-thio-ether) forms a five-membered dimetalla-cyclo-pentenone ring, in which the C=C bond is π-coordinated to the Fe center. The latter is connected to the Pt center through a short metal-metal bond of 2.5697 (6) Å.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336804PMC
http://dx.doi.org/10.1107/S2056989020007859DOI Listing

Publication Analysis

Top Keywords

crystal structure
4
structure {μ-12-bis-[4-methyl-phenyl-sulfan-yl]-3-oxoprop-1-ene-13-di-yl-12κ
4
{μ-12-bis-[4-methyl-phenyl-sulfan-yl]-3-oxoprop-1-ene-13-di-yl-12κ }dicarbon-yl-1κ
4
}dicarbon-yl-1κ -[μ-methyl-enebisdi-phenyl-phos-phane-12κ
4
-[μ-methyl-enebisdi-phenyl-phos-phane-12κ ']tri-phenyl-phosphane-2κiron-platinum-
4
']tri-phenyl-phosphane-2κiron-platinum- [ocfeμ-dppm{μ-c=oc4-mechsch=cchschme-4}ptpph]
4
[ocfeμ-dppm{μ-c=oc4-mechsch=cchschme-4}ptpph] title
4
title compound
4
compound [feptchoschpchpco]
4
[feptchoschpchpco] [ocfeμ-dppmμ-c=occhschme-4=cchschme-4ptpph]
4

Similar Publications

The matere bond.

Dalton Trans

January 2025

Department of Chemistry, Universitat de les Illes Balears, Crta de Valldemossa km 7.5, 07122 Palma de Mallorca, Baleares, Spain.

This perpective delves into the emerging field of matere bonds, a novel type of noncovalent interaction involving group 7 elements such as manganese, technetium, and rhenium. Matere bonds, a new member of the σ-hole family where metal atoms act as electron acceptors, have been shown experimentally and theoretically to play significant roles in the self-assembly and stabilization of supramolecular structures both in solid-state and solution-phase environments. This perspective article explores the physical nature of these interactions, emphasizing their directionality and structural influence in various supramolecular architectures.

View Article and Find Full Text PDF

Monoprotonated species of 2-aminomalonyl difluoride, [CHFNO][HF].

Acta Crystallogr C Struct Chem

February 2025

Department Chemie, Ludwig-Maximilians Universität, Butenandtstrasse 5-13 (Haus D), D-81377 München, Germany.

The monoprotonated species of 2-aminomalonyl difluoride, namely, 1,3-difluoro-1,3-dioxopropan-2-aminium dihydrogen trifluoride, [CHFNO][HF], was synthesized from sulfur tetrafluoride in anhydrous hydrogen fluoride (aHF) with [NH][CHNO] as the starting material. The solvent was removed and the salt was dissolved in aHF and crystallized. In the solid state, the three-dimensional network is built by medium-strong N-H.

View Article and Find Full Text PDF

In this work, coixalkyne A (), a natural polynuclear calcium complex with a novel cross-shaped molecular architecture, was isolated from L. along with the undescribed analogue coixalkyne B (). Their structures were identified by means of NMR spectroscopy, ECD calculations, and single-crystal X-ray diffraction.

View Article and Find Full Text PDF

Steam explosion (SE) and cellulase treatment are potentially effective processing methods for by-products, for use in high-value applications. The treatment conditions were optimized by response surface methodology, increasing the soluble dietary fiber (SDF) yield by 1.52 and 1.

View Article and Find Full Text PDF

The layer-stacking mode of a two-dimensional (2D) material plays a dominant role either in its topology or properties, but remains challenging to control. Herein, we developed alkali-metal ion-regulating synthetic control on the stacking structure of a vinylene-linked covalent triazine framework (termed spc-CTF) for improving hydrogen peroxide (HO) photoproduction. Upon the catalysis of EtONa in Knoevenagel polycondensation, a typical eclipsed stacking mode (spc-CTF-4@AA) was built, while a staggered one (spc-CTF-4@AB) was constructed using LiOH.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!