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Organic-inorganic hybrid thiocyanates include a variety of compositions and structure types. To develop a better understanding of the interactions that control the crystal structure in this family of materials, six hybrid thiocyanate halide compounds with the general formula ACd(SCN)X (A = CHNH, CHCHNH, CH(CH)NH, CH(CH)NH; X = Cl, Br) have been synthesized. Single crystal X-ray diffraction shows that five of the six compounds crystallize with triclinic 1̅ symmetry, the lone exception being (CH(CH)NH)Cd(SCN)Cl which adopts 2/ symmetry. Thermal analysis reveals decomposition temperatures between 180 and 210 °C. The intermediate hard-soft acidic nature of Cd favors bridging thiocyanate groups and lowers the dimensionality compared to their Pb and Sn analogues, which adopt two-dimensional crystal structures with bridging halide ions. The presence of bridging thiocyanate groups lead to one-dimensional chains of [Cd(SCN)X] octahedra. Hydrogen bonding interactions between terminal halide ions and the amine headgroup of the organic cation dictate the crystal packing and play a key role in determining the thermal stability of these compounds. Diffuse reflectance measurements reveal large band gaps, ranging from 3.7 to 4.4 eV, and electronic structure calculations reveal narrow bands, with dispersions on the order of 0.5 eV. These attributes are likely to be characteristic of compounds with bridging thiocyanate linkers.
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http://dx.doi.org/10.1021/acs.inorgchem.5c01639 | DOI Listing |
Inorg Chem
September 2025
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Organic-inorganic hybrid thiocyanates include a variety of compositions and structure types. To develop a better understanding of the interactions that control the crystal structure in this family of materials, six hybrid thiocyanate halide compounds with the general formula ACd(SCN)X (A = CHNH, CHCHNH, CH(CH)NH, CH(CH)NH; X = Cl, Br) have been synthesized. Single crystal X-ray diffraction shows that five of the six compounds crystallize with triclinic 1̅ symmetry, the lone exception being (CH(CH)NH)Cd(SCN)Cl which adopts 2/ symmetry.
View Article and Find Full Text PDFMolecules
June 2025
Chemistry, Department of Biology/Chemistry, Osnabrück University, Barbarastr. 7, D 49069 Osnabrück, Germany.
As part of a systematic study on the structures of the mixed halide isothiocyanates, SnHal(NCS), their single crystals were grown and structurally characterized. For Hal = F (), the SnClF structure type was confirmed, while with Hal = Cl (), Br (), and I (), there are three isostructural compounds of a new structure type, and for Hal = Cl (), there is a second modification of a third structure type. These structure types have been described with respect to the composition and coordination geometry of the first, second, and van der Waals crust coordination spheres and their dependence on the halogen size and thiocyanate binding modes.
View Article and Find Full Text PDFChem Commun (Camb)
July 2025
Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun 130024, China.
The rational design and synthesis of donor-π-acceptor (D-π-A) type tetraphenylsilane (TEPS)-based PAFs (PAF-403, PAF-404, and PAF-405) linked by acetylene bridges are presented. Among them, PAF-405 displays the highest efficiency for visible-light-induced C-3 thiocyanation of indoles (up to 99% yield) with broad substrate scope (15 examples), which could be recycled for five cycles with a slight loss of catalytic activity. A possible structure-performance correlation of TEPS-PAFs is proposed.
View Article and Find Full Text PDFDalton Trans
April 2025
Instituto de Ciencia Molecular (ICMol), Universidad de Valencia, Catedrático José Beltrán Martínez, 2, 46980 Paterna, Valencia, Spain.
While halide substitution has significantly influenced the electrical and magnetic properties of α-layered hydroxide frameworks (α-LH), the incorporation of pseudohalides remains limited. In this study, we present a detailed investigation of two-dimensional cobalt-layered hydroxides modified with tricyanomethanide (CN) and thiocyanate (SCN) pseudohalides, synthesized a simple epoxide route at room temperature. Pseudohalide incorporation induces subtle structural modifications relative to pristine cobalt-chloride layered hydroxide (α-Co-Cl), including changes in interlayer spacing and the confirmation of a distinct bridging coordination in thiocyanate-modified samples.
View Article and Find Full Text PDFAnal Chem
January 2025
Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, Indiana 47405, United States.
Two-dimensional infrared (2D IR) spectroscopy is a powerful technique for measuring molecular heterogeneity and dynamics with a high spatiotemporal resolution. The methods can be applied to characterize specific residues of proteins by incorporating frequency-resolved vibrational labels. However, the time scale of dynamics that 2D IR spectroscopy can measure is limited by the vibrational label's excited-state lifetime due to the decay of 2D IR absorption bands.
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