Hydrides in metal complexes or nanoclusters are typically viewed as electron-withdrawing. Several recent reports have demonstrated the emergence of "electron-donating" hydrides in tailoring the structure, electronic structure, and reactivity of metal nanoclusters. However, the number of such hydrides included in each cluster kernel is limited to one or two. There is even no structure model, neither theoretical nor experimental, for encapsulating a third electron-donating hydride into one cluster entity. Here, we present a structurally precise superatomic nanocluster, PtHCu(iso-propyl-PhS)(PPh) (PtHCu), which contains three interstitial electron-donating hydrides. The molecular structure of PtHCu describes the encapsulation of a PtCu core that contains three interstitial hydrides in a distorted anticuboctahedral architecture, in an outer sphere consisting of copper atoms and thiolate and phosphine ligands. Density functional theory calculations reveal that the three hydrides in PtHCu contribute their valence electrons to the cluster superatomic electron count of eight. In this regard, the cluster represents a rare Pt-included copper-hydride superatom with eight free electrons.
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http://dx.doi.org/10.1126/sciadv.ads4488 | DOI Listing |
Sci Adv
January 2025
College of Energy Materials and Chemistry, Inner Mongolia University, Hohhot 010021, China.
Hydrides in metal complexes or nanoclusters are typically viewed as electron-withdrawing. Several recent reports have demonstrated the emergence of "electron-donating" hydrides in tailoring the structure, electronic structure, and reactivity of metal nanoclusters. However, the number of such hydrides included in each cluster kernel is limited to one or two.
View Article and Find Full Text PDFChem Sci
December 2024
School of Materials Science and Engineering, PCFM Lab, the Key Laboratory of Low-carbon Chemistry & Energy Conservation of Guangdong Province, Sun Yat-sen University Guangzhou 510006 P. R. China
Metal-ligand cooperation (MLC) is an essential strategy in transition metal catalysis. Traditional NH-based and OH-based MLC catalysts, as well as the later developed (de)aromatization strategy, have been widely applied in atom-economic borrowing hydrogen/hydrogen auto-transfer (BH/HA) reactions. However, these conventional MLC approaches are challenging for low-coordination and low-activity coinage metal complexes, arising from the instability during (de)protonation on the coordination atom, the constraint in linear coordination, and possible poisoning due to extra functional sites.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemistry, Faculty of Science, Kyushu University, Motooka 744, Nishi-ku, Fukuoka 819-0395, Japan.
Photocatalytic reduction of CO to formic acid (HCOOH) was investigated in either organic or aqueous/organic media by employing three water-soluble [RhCp*(LH)Cl] (LH = n,n'-dihydroxy-2,2'-bipyridine; = 4, 5, or 6) in the presence of [Ru(bpy)], 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[]imidazole (BIH) and triethanolamine (TEOA). Through studying the electron-donating effects of two hydroxyl groups introduced into the bipyridyl ligand, we found that the substituent positions greatly affect both the catalytic efficiency and selectivity in CO reduction. More importantly, the HCOOH selectivity shows a dramatic increase from 14 to 83% upon switching the solvent media from pure organic to an aqueous/organic mixture, where the H selectivity shows a reverse phenomenon.
View Article and Find Full Text PDFChemistry
November 2024
Department of Chemical Sciences, Indian Institute of Science Education and Research Mohali, Knowledge City, Sector 81, SAS Nagar, Mohali, Punjab, 140306, India.
Hydride abstraction from the borane adduct, (BICAAC) ⋅ BH afforded the hydride bridged dinuclear borenium ion equivalent complexes 1 and 2 that have been characterized by various spectroscopic and spectrometric techniques followed by the assessment of Lewis acidity using the Gutmann-Beckett method. The single crystal X-ray structure of complex 2 revealed the presence of discrete ions in the solid state. The complex (BICAAC) ⋅ BH(OTf) (3), obtained from the reaction of (BICAAC) ⋅ BH with MeOTf, formed the corresponding boronium cations [(BICAAC) ⋅ BH(L)](OTf) on reaction with Lewis bases (L= pyridine (4) and DMAP (5)).
View Article and Find Full Text PDFAcc Chem Res
October 2024
The Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States.
ConspectusDespite the plethora of metal catalyzed reactions for CO utilization that have been developed in academic laboratories, practical systems remain elusive. The understanding of the elementary steps in catalysis is a proven method to improve catalytic performance. In many catalytic cycles for CO utilization, the insertion of CO into a metal-element σ-bond, such as hydrides, alkyls, amides, or hydroxides, is a crucial step.
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