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Structural Resilience in Organic-Inorganic Stacked Assemblies: Sulfur-Mediated Self-Compensating Interaction and Metal Identity Masking in Group 10 Dithiocarbamate Cocrystals with Tetracyanobenzene Full article

Journal Inorganic Chemistry Frontiers
ISSN: 2052-1553 , E-ISSN: 2052-1545
Output data Year: 2026, Volume: 13, Number: 1, Pages: 232-245 Pages count : 14 DOI: 10.1039/D5QI01980J
Authors Zelenkov Lev E. 1 , Baykov Sergey V. 2 , Kuznetsov Maxim L. 3 , Sadykov Evgeny Kh. 4 , Nikul’shin Pavel V. 5,6 , Ignatov Eugene V. 2,7 , Bokach Nadezhda A. 2 , Kukushkin Vadim Yu. 2,7
Affiliations
1 Qingdao Innovation and Development Center, Harbin Engineering University, Qingdao 266000, Shandong, China
2 Institute of Chemistry, Saint Petersburg State University, Universitetskaya Nab. 7/9, 199034 Saint Petersburg, Russian Federation
3 Centro de Química Estrutural, Institute of Molecular Sciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal
4 Laboratory of Physical Chemistry of Condensed Matter, A. V. Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Av. 3, 630090 Novosibirsk, Russian Federation
5 A.N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, 28 Vavilova St., 119991 Moscow, Russian Federation
6 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9, Lavrentiev Av., 630090 Novosibirsk, Russian Federation
7 Institute of Chemistry and Pharmaceutical Technologies, Altai State University, Lenin Av. 61, 656049 Barnaul, Russian Federation

Abstract: This work investigates the relative influence of metal identity versus ligand environment in determining supramolecular architecture of stacked hybrid organic–inorganic systems. We demonstrate a sulfurmediated self-compensating mechanism that masks metal-specific electronic differences, enabling ligand-controlled assembly over conventional metal-directed organization. Through systematic investigation of group 10 metal dithiocarbamate cocrystals [M(S2CNR2)2] (M = Ni, Pd, Pt; R2 = alkyl) with 1,2,4,5tetracyanobenzene, we reveal structural resilience—identical parallel-displaced supramolecular architectures are maintained across the entire Ni–Pd–Pt triad despite fundamental differences in dz2-orbital nucleophilicity that typically govern such assemblies. This contradicts established principles where metal variation should produce distinctly different structural outcomes. Comprehensive quantum chemical analysis using QTAIM, IGM, ETS-NOCV, and energy decomposition methods reveals that S atoms from the dithiocarbamate ligands actively neutralize inherent metal-specific properties, creating electronically equivalent {MS4} building blocks. Despite different metals, remarkably consistent interaction energies (−40.6 to −42.8 kcal mol−1) and metal contributions (13.9–15.9%) demonstrate functional equivalence in the supramolecular recognition. Our study establishes ligand-mediated metal identity masking as a design principle for creating structurally predictable metal-involving materials regardless of metal center.
Cite: Zelenkov L.E. , Baykov S.V. , Kuznetsov M.L. , Sadykov E.K. , Nikul’shin P.V. , Ignatov E.V. , Bokach N.A. , Kukushkin V.Y.
Structural Resilience in Organic-Inorganic Stacked Assemblies: Sulfur-Mediated Self-Compensating Interaction and Metal Identity Masking in Group 10 Dithiocarbamate Cocrystals with Tetracyanobenzene
Inorganic Chemistry Frontiers. 2026. V.13. N1. P.232-245. DOI: 10.1039/D5QI01980J WOS Scopus
Dates:
Submitted: Sep 26, 2025
Accepted: Oct 18, 2025
Published online: Oct 21, 2025
Published print: Jan 6, 2026
Identifiers:
Web of science: WOS:001600469200001
Scopus: 2-s2.0-105026445967
Citing: Пока нет цитирований
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