Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4and Au@Ag4Clusters Supported by tris(2-Pyridyl)phosphine

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Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu₄and Au@Ag₄Clusters Supported by tris(2-Pyridyl)phosphine. / Baranov, Andrey Yu; Slavova, Sofia O.; Berezin, Alexey S.; Petrovskii, Stanislav K.; Samsonenko, Denis G.; Bagryanskaya, Irina Yu; Fedin, Vladimir P.; Grachova, Elena V.; Artem'Ev, Alexander V.

в: Inorganic Chemistry, Том 61, № 28, 18.07.2022, стр. 10925-10933.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Author

Baranov, Andrey Yu ; Slavova, Sofia O. ; Berezin, Alexey S. ; Petrovskii, Stanislav K. ; Samsonenko, Denis G. ; Bagryanskaya, Irina Yu ; Fedin, Vladimir P. ; Grachova, Elena V. ; Artem'Ev, Alexander V. / Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu₄and Au@Ag₄Clusters Supported by tris(2-Pyridyl)phosphine. в: Inorganic Chemistry. 2022 ; Том 61, № 28. стр. 10925-10933.

BibTeX

@article{30687d3c1f18421e8053f6b32468b9d7,

title = "Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4and Au@Ag4Clusters Supported by tris(2-Pyridyl)phosphine",

abstract = "We report herein a family of polynuclear complexes, [Au@Ag4(Py3P)4]X5 and [Au@Cu4(Py3P)4]X5 [X = NO3, ClO4, OTf, BF4, SbF6], containing unprecedented Au-centered Ag4 and Cu4 tetrahedral cores supported by tris(2-pyridyl)phosphine (Py3P) ligands. The [Au@Ag4]5+ clusters are synthesized via controlled substitution of the central Ag(I) ion in all-silver [Ag@Ag4]5+ precursors by the reaction with Au(tht)Cl, while the [Au@Cu4]5+ cluster is assembled through the treatment of a pre-organized [Au(Py3P)4]+ metallo-ligand with 4 equiv of a Cu(I) source. The structure of the Au@M4 clusters has been experimentally and theoretically investigated to reveal very weak intermolecular Au-M metallophilic interactions. At ambient temperature, the designed compounds emit a modest turquoise-to-yellow luminescence with microsecond lifetimes. Based on the temperature-dependent photophysical experiments and DFT/TD-DFT computations, the emission observed has been assigned to an MLCT or LLCT type depending on composition of the cluster core.",

author = "Baranov, {Andrey Yu} and Slavova, {Sofia O.} and Berezin, {Alexey S.} and Petrovskii, {Stanislav K.} and Samsonenko, {Denis G.} and Bagryanskaya, {Irina Yu} and Fedin, {Vladimir P.} and Grachova, {Elena V.} and Artem'Ev, {Alexander V.}",

note = "Publisher Copyright: {\textcopyright} 2022 American Chemical Society.",

year = "2022",

month = jul,

day = "18",

doi = "10.1021/acs.inorgchem.2c01474",

language = "English",

volume = "61",

pages = "10925--10933",

journal = "Inorganic Chemistry",

issn = "0020-1669",

publisher = "American Chemical Society",

number = "28",

}

RIS

TY - JOUR

T1 - Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4and Au@Ag4Clusters Supported by tris(2-Pyridyl)phosphine

AU - Baranov, Andrey Yu

AU - Slavova, Sofia O.

AU - Berezin, Alexey S.

AU - Petrovskii, Stanislav K.

AU - Samsonenko, Denis G.

AU - Bagryanskaya, Irina Yu

AU - Fedin, Vladimir P.

AU - Grachova, Elena V.

AU - Artem'Ev, Alexander V.

PY - 2022/7/18

Y1 - 2022/7/18

N2 - We report herein a family of polynuclear complexes, [Au@Ag4(Py3P)4]X5 and [Au@Cu4(Py3P)4]X5 [X = NO3, ClO4, OTf, BF4, SbF6], containing unprecedented Au-centered Ag4 and Cu4 tetrahedral cores supported by tris(2-pyridyl)phosphine (Py3P) ligands. The [Au@Ag4]5+ clusters are synthesized via controlled substitution of the central Ag(I) ion in all-silver [Ag@Ag4]5+ precursors by the reaction with Au(tht)Cl, while the [Au@Cu4]5+ cluster is assembled through the treatment of a pre-organized [Au(Py3P)4]+ metallo-ligand with 4 equiv of a Cu(I) source. The structure of the Au@M4 clusters has been experimentally and theoretically investigated to reveal very weak intermolecular Au-M metallophilic interactions. At ambient temperature, the designed compounds emit a modest turquoise-to-yellow luminescence with microsecond lifetimes. Based on the temperature-dependent photophysical experiments and DFT/TD-DFT computations, the emission observed has been assigned to an MLCT or LLCT type depending on composition of the cluster core.

AB - We report herein a family of polynuclear complexes, [Au@Ag4(Py3P)4]X5 and [Au@Cu4(Py3P)4]X5 [X = NO3, ClO4, OTf, BF4, SbF6], containing unprecedented Au-centered Ag4 and Cu4 tetrahedral cores supported by tris(2-pyridyl)phosphine (Py3P) ligands. The [Au@Ag4]5+ clusters are synthesized via controlled substitution of the central Ag(I) ion in all-silver [Ag@Ag4]5+ precursors by the reaction with Au(tht)Cl, while the [Au@Cu4]5+ cluster is assembled through the treatment of a pre-organized [Au(Py3P)4]+ metallo-ligand with 4 equiv of a Cu(I) source. The structure of the Au@M4 clusters has been experimentally and theoretically investigated to reveal very weak intermolecular Au-M metallophilic interactions. At ambient temperature, the designed compounds emit a modest turquoise-to-yellow luminescence with microsecond lifetimes. Based on the temperature-dependent photophysical experiments and DFT/TD-DFT computations, the emission observed has been assigned to an MLCT or LLCT type depending on composition of the cluster core.

UR - http://www.scopus.com/inward/record.url?scp=85134631868&partnerID=8YFLogxK

U2 - 10.1021/acs.inorgchem.2c01474

DO - 10.1021/acs.inorgchem.2c01474

M3 - Article

C2 - 35775806

AN - SCOPUS:85134631868

VL - 61

SP - 10925

EP - 10933

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 28

ER -

ID: 97614153