In this study, the stability, directionality, and physical nature of Spodium bonds (SpBs, an attractive noncovalent force involving elements from group 12 and Lewis bases) between methylmercury (MeHg) and ethylmercury (EtHg) and amino acids (AAs) have been analyzed from both a structural (X-ray analysis) and theoretical (RI-MP2/def2-TZVP level of theory) point of view. More in detail, an inspection of the Protein Data Bank (PDB) reported evidence of noncovalent contacts between MeHg and EtHg molecules and electron-rich atoms (e.g., O atoms belonging to the protein backbone and S atoms from MET residues or the π-systems of aromatic AAs such as TYR or TRP). These results were rationalized through a computational study using MeHg coordinated to a thiolate group as a theoretical model and several neutral and charged electron-rich molecules (e.g., benzene, formamide, or chloride). The physical nature of the interaction was analyzed from electrostatics and orbital perspectives by performing molecular electrostatic potential (MEP) and natural bonding orbital (NBO) analyses. Lastly, the noncovalent interactions plot (NCIplot) technique was used to provide a qualitative view of the strength of the Hg SpBs and compare them to other ancillary interactions present in these systems as well as to shed light on the extension of the interaction in real space. We believe that the results derived from our study will be useful to those scientists devoted to protein engineering and bioinorganic chemistry as well as to expanding the current knowledge of SpBs among the chemical biology community.
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http://dx.doi.org/10.1021/acs.inorgchem.3c02716 | DOI Listing |
Chempluschem
December 2024
Indian Institute of Technology Jodhpur, Chemistry, Jodhpur, 342037, Jodhpur, INDIA.
Herein, we present a distorted square pyramidal mercury complex, [HgII(L)Cl] (1), based on a quinoline-substituted formazan ligand LH[3-Cyano-1,5-(quinolin-8-yl)formazan], which was evaluated for its anti-bacterial activity in vitro. Complex 1 was prepared by refluxing 3-Cyano-1,5-(quinolin-8-yl)formazan ligand and mercury chloride(II) in equimolar quantity and was characterized utilizing a range of analytical methods, including single crystal X-ray diffraction (SCXRD) technique. The crystal packing in complex 1 has been elucidated using supramolecular investigations, which have shown the presence of fascinating Hg-Cl···Hg intermolecular spodium bonds of the order 3.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Department of Chemistry, Pondicherry University, Pondicherry, 605014, India.
Statistical analyses and computational studies have been performed on spodium bonds with four- and five-coordinated spodium complexes. Though statistical analyses without geometry correction suggest that the most populous geometries are far from linearity, geometry-corrected analyses suggest that these bonds are directional and linear. Computational studies suggest that the bond strength can be moderately strong.
View Article and Find Full Text PDFACS Omega
October 2024
Department of Chemistry, Jadavpur University, Kolkata 700032, India.
Two tridentate N,N,O-donor ligands, HL = 4-chloro-2-(((2-(methylamino)ethyl)amino)methyl)phenol and HL = 4-chloro-2-(((2-(dimethylamino)ethyl)amino)methyl)phenol, have been used to synthesize phenolate-bridged dinuclear complexes [Zn(L)Cl] () and [Zn(L)(N)] (). Single-crystal X-ray diffraction analysis confirmed their structures. Both complexes form assemblies in the solid state.
View Article and Find Full Text PDFJ Phys Chem A
October 2024
Department of Chemistry and Biochemistry, Utah State University Logan, Logan, Utah 84322-0300, United States.
DFT calculations consider the interactions between linear MR and a series of N-bases, where M is Hg or Zn and its R substituents are CCH, CN, or NO. NCH, NH, and NMe were considered as three different N-bases. Zn forms stronger bonds with the N bases than does Hg, and they strengthen along with the electron-withdrawing power of the R substituent, varying over a wide range from 3.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Amity Institute of Click Chemistry Research and Studies, Amity University, Noida, Uttar Pradesh, India.
Herein we have evidenced the formation of favorable π-hole Br⋅⋅⋅metal noncovalent interactions (NCIs) involving elements from groups 9, 11 and 12. More in detail, M (M=Co, Ni, Cu and Zn) containing porphyrins have been synthesized and their supramolecular assemblies structurally characterized by means of single crystal X-ray diffraction and Hirshfeld surface analyses, revealing the formation of directional Br⋅⋅⋅M contacts in addition to ancillary hydrogen bond and lone pair-π bonds. Computations at the PBE0-D3/def2-TZVP level of theory revealed the π-hole nature of the Br⋅⋅⋅M interaction.
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