7 research outputs found
Magnesium cinnamate complex, [Mg(cinn)2(H2O)2]n; structural, spectroscopic, thermal, biological and pharmacokinetical characteristics
Microstructural, electronic, and mechanical properties of Al4La and Al4Sm intermetallics: An experimental and first-principles calculations
A new potassium-based coordination polymer with hydrogen bonding and zigzag metallophilic interactions
Sonochemical synthesis of a two-dimensional supramolecular polymer with nanoporous morphology, linear thallophilic and covalent hydrogen-bonding interactions
Metallophilic Mercuraazamacrocycles Derived from Bis{6-formyl-(2,3,4-trimethoxy)phenyl}mercury: Reactivity with d 10
Structural Diversity and Argentophilic Interactions in Small Phosphine Silver(I) Thiolate Clusters
10 pags., 5 figs., 4 tabs.Silver(I) coordination compounds display an interesting geometrical diversity, the possibility of having distinct coordination numbers (typically from 2 to 4) and the capability of forming argentophilic (Ag⋅⋅⋅Ag) interactions. These properties complicate the accurate prediction of structures of silver complexes under certain experimental conditions. In this work, we show how subtle modifications in thiolate and phosphine ligands exert important effects on the nuclearity and geometry of phosphine caped clusters [Ag(SR)] (n=4, 6 and 8). We rationalize these effects in terms of the electronic environment of silver centers by analyzing the electronic density of the single-crystal X-ray structures via the Quantum Theory of Atoms in Molecules (QTAIM) and the Non-Covalent Interaction (NCI)-Index. Furthermore, we characterized attractive and repulsive argentophilic contacts by means of the Interacting Quantum Atoms (IQA) energy partition. Our results provide insights on the effects of ancillary ligands in controlling the structure of silver-thiolate clusters. Such control is relevant towards a bottom-up approach to the atomic precise construction of higher nuclearity clusters.We acknowledge fundingby DGAPA-UNAM project IN210818,andby CONACYT-Mexico through the postdoctoral grant 740732. We are also thankful for the instrumental support of the Unit for Industryand Research Support (USAII)at the School of Chemistry at UNAM, Mexico and for the computer time provided by DGTIC/UNAMproject LANCAD-DGTIC-UNAM-250.G.M.-A acknowledges the RSC-Chemists’CommunityFund suppor