Inorganic-organic {dz2-MIIS4}⋯π-hole stacking in reverse sandwich structures: the case of cocrystals of group 10 metal dithiocarbamates with electron-deficient arenes; Inorganic Chemistry Frontiers; Vol. 9, iss. 12

Bibliographic Details
Parent link:Inorganic Chemistry Frontiers
Vol. 9, iss. 12.— 2022.— [P. 2869-2879]
Corporate Author: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий Международная научно-исследовательская лаборатория "Невалентные взаимодействия в химии материалов"
Other Authors: Zelenkov L. E. Lev, Eliseeva A. A. Anastasiya, Baykov S. V. Sergey Valentinovich, Ivanov D. M. Daniil Mikhaylovich, Sumina A. I. Alina Ivanovna, Rosa M. G. Maria Gomila, Frontera A. Antonio, Kukushkin V. Yu. Vadim Yurjevich, Bokach N. A. Nadezhda Arsenjevna
Summary:Title screen
Cocrystallization of the dithiocarbamate complexes [M(S2CNEt2)2] (M = Ni 1, Pd 2, Pt 3) and X-substituted perfluoroarenes (X = I, Br; 1,2-dibromoperfluorobenzene FBrB and 1,2-diiodoperfluorobenzene FIB) gives isomorphous cocrystals of (1-3)·2(FBrB) and 1·2(FIB), correspondingly, whose structures were studied by single-crystal X-ray diffractometry. The crystal structures demonstrate similar intermolecular contact types: short arene MS4⋯π-hole stacking contacts, X⋯S halogen bonds, C-H⋯X (X = Br, I) bonds and C-H⋯F hydrogen bonds. In these structures, the {dz2-MIIS4} moiety functions as an integrated five-center acceptor (that includes a metal dz2-orbital, even for a poorly dz2-nucleophilic NiII center) toward the π-hole of an X-substituted perfluoroarene. This interaction provides stacking of inorganic and organic units furnishing the reverse sandwich structures. Density functional theory (DFT) calculations, in combination with quantum theory of atoms-in-molecules (QTAIM) and noncovalent interaction plot (NCIplot) analyses, supported the structure-defining role of the {MS4}⋯π-hole contacts. The nucleophilicity of the {MS4} cores toward electron deficient π-holes was verified from the molecular electrostatic potential surface (MEP) and electron density/electrostatic potential (ED/ESP) profiles, and atoms-in-molecules (AIM) charge analysis. The relatively strong {MS4}⋯π-hole contact strength (interaction energies for an {MS4}⋯π-hole 1 : 1 adduct range from −12.1 to −13.5 kcal mol−1) is probably due to the large overlap between the electron deficient π-cloud and the integrated {MS4} nucleophilic core. The 1 : 1 adduct based on 3 demonstrates the largest strength (13.5 kcal mol−1) in the series and this strength agrees well with the higher dz2-nucleophilicity of the PtII center revealed by the MEP analysis (−33.6 kcal mol−1).
Language:English
Published: 2022
Subjects:
Online Access:https://doi.org/10.1039/D2QI00438K
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=668202

MARC

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200 1 |a Inorganic-organic {dz2-MIIS4}⋯π-hole stacking in reverse sandwich structures: the case of cocrystals of group 10 metal dithiocarbamates with electron-deficient arenes  |f L. E. Zelenkov, A. A. Eliseeva, S. V. Baykov [et al.] 
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300 |a Title screen 
330 |a Cocrystallization of the dithiocarbamate complexes [M(S2CNEt2)2] (M = Ni 1, Pd 2, Pt 3) and X-substituted perfluoroarenes (X = I, Br; 1,2-dibromoperfluorobenzene FBrB and 1,2-diiodoperfluorobenzene FIB) gives isomorphous cocrystals of (1-3)·2(FBrB) and 1·2(FIB), correspondingly, whose structures were studied by single-crystal X-ray diffractometry. The crystal structures demonstrate similar intermolecular contact types: short arene MS4⋯π-hole stacking contacts, X⋯S halogen bonds, C-H⋯X (X = Br, I) bonds and C-H⋯F hydrogen bonds. In these structures, the {dz2-MIIS4} moiety functions as an integrated five-center acceptor (that includes a metal dz2-orbital, even for a poorly dz2-nucleophilic NiII center) toward the π-hole of an X-substituted perfluoroarene. This interaction provides stacking of inorganic and organic units furnishing the reverse sandwich structures. Density functional theory (DFT) calculations, in combination with quantum theory of atoms-in-molecules (QTAIM) and noncovalent interaction plot (NCIplot) analyses, supported the structure-defining role of the {MS4}⋯π-hole contacts. The nucleophilicity of the {MS4} cores toward electron deficient π-holes was verified from the molecular electrostatic potential surface (MEP) and electron density/electrostatic potential (ED/ESP) profiles, and atoms-in-molecules (AIM) charge analysis. The relatively strong {MS4}⋯π-hole contact strength (interaction energies for an {MS4}⋯π-hole 1 : 1 adduct range from −12.1 to −13.5 kcal mol−1) is probably due to the large overlap between the electron deficient π-cloud and the integrated {MS4} nucleophilic core. The 1 : 1 adduct based on 3 demonstrates the largest strength (13.5 kcal mol−1) in the series and this strength agrees well with the higher dz2-nucleophilicity of the PtII center revealed by the MEP analysis (−33.6 kcal mol−1). 
461 |t Inorganic Chemistry Frontiers 
463 |t Vol. 9, iss. 12  |v [P. 2869-2879]  |d 2022 
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701 1 |a Eliseeva  |b A. A.  |g Anastasiya 
701 1 |a Baykov  |b S. V.  |c chemist  |c Researcher at Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1987-  |g Sergey Valentinovich  |3 (RuTPU)RU\TPU\pers\47276 
701 1 |a Ivanov  |b D. M.  |c Chemist  |c Senior researcher of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1992-  |g Daniil Mikhaylovich  |3 (RuTPU)RU\TPU\pers\47038 
701 1 |a Sumina  |b A. I.  |g Alina Ivanovna 
701 1 |a Rosa  |b M. G.  |g Maria Gomila 
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701 1 |a Kukushkin  |b V. Yu.  |g Vadim Yurjevich 
701 1 |a Bokach  |b N. A.  |c Chemist  |c Leading researcher of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1976-  |g Nadezhda Arsenjevna  |3 (RuTPU)RU\TPU\pers\47040 
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