- Main
Supramolecular Support of Cuprophilic Network Bonding in 2‑D Copper n‑Alkanethiolates
- Willson, Maggie C;
- Paley, Daniel W;
- Schriber, Elyse A;
- Rosenberg, Daniel J;
- Tchoń, Daniel M;
- Kotei, Patience A;
- Rani, Komal;
- Melendrez, Cynthia;
- Zeller, Matthias;
- Kaushik, Tarun;
- Fan, Qiaoling;
- Liyanage, Chamathka Dehiwala;
- Kang, Jungmin;
- Inoue, Ichiro;
- Tono, Kensuke;
- Inubushi, Yuichi;
- Brewster, Aaron S;
- Hohman, J Nathan
Published Web Location
https://doi.org/10.1021/acs.inorgchem.5c02024Abstract
The development of heterogeneous materials, catalysts, and semiconductors is often reliant on precise control of self-assembly and crystal packing. Many new materials are initially synthesized as microcrystalline powders, making them incompatible with typical methods of structure determination, such as single-crystal X-ray diffraction. This resultant lack of structural information has made thorough investigation into the effect of metal substitution on crystal structure in metal-organic chalcogenolates (MOChas) challenging. Here, we use small molecule serial femtosecond crystallography (smSFX) to present the structures of four copper n-alkanethiolates: CuSC4, CuSC5, CuSC6, and CuSC7. Divergent patterns of alkyl chain packing are identified from microcrystalline powders via smSFX. An odd-even effect in crystal packing has been identified and attributed to different orientations of symmetry elements in the even- and odd-numbered chains. This results in minute changes in the azimuthal organization of the even-numbered chains and the network of cuprophilic interactions. Additionally, we present a synthesis of crystalline gold n-alkanethiolates to provide the first comparison between three d10 coinage metals (Cu, Ag, and Au) and their resultant n-alkanethiolates.
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