Structural Diversity and Argentophilic Interactions in One-Dimensional Silver-Based Coordination Polymers
Source abstract
Abstract
A series of new one-dimensional coordination polymer materials, based on Ag(I)–N bond formation, has been synthesized and structurally characterized by single crystal X-ray diffraction. Reactions between the poly-monodentate ligands based on ( 1E, 1 ′ E ′) -N, N ′ - (-bis(1-pyridin-3-yl)methanimine and Ag(I) salts give products that feature simple coordination chains or metallacyclic- and tape-based structures. For the simple chains these are as either isolated units, or assembled in dimeric and tetrameric arrangements through intermetallic, argentophilic interactions. However, crystal packing effects and solvent inclusion are found to readily disrupt this type of bonding. Density functional theory calculations provide an assessment of the bond order and the influence of anion binding on these interactions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Metal complexes synthesis and properties · Magnetism in coordination complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemical Nanoscience Laboratory, School of Chemistry, Newcastle University, Newcastle upon Tyne, NE1 7RU, U.K.
School of Chemistry, Newcastle University, Newcastle upon Tyne, NE1 7RU, U.K.
Crystallography Laboratory, School of Chemistry, Newcastle University, Newcastle upon Tyne, NE1 7RU, U.K.
Funding
Engineering and Physical Sciences Research Council · School of Chemistry, Newcastle University · Akzo Nobel N.V.
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