Standard

Synthesis of bismuthanyl-substituted monomeric triel hydrides. / Szlosek, Robert; Marquardt, Christian; Hegen, Oliver; Balazs, Gabor; Riesinger, Christoph; Тимошкин, Алексей Юрьевич; Scheer, M.

в: Chemical Science, Том 15, № 36, D4SC03926B, 12.08.2024, стр. 14837-14843.

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

Harvard

Szlosek, R, Marquardt, C, Hegen, O, Balazs, G, Riesinger, C, Тимошкин, АЮ & Scheer, M 2024, 'Synthesis of bismuthanyl-substituted monomeric triel hydrides', Chemical Science, Том. 15, № 36, D4SC03926B, стр. 14837-14843. https://doi.org/10.1039/D4SC03926B

APA

Szlosek, R., Marquardt, C., Hegen, O., Balazs, G., Riesinger, C., Тимошкин, А. Ю., & Scheer, M. (2024). Synthesis of bismuthanyl-substituted monomeric triel hydrides. Chemical Science, 15(36), 14837-14843. [D4SC03926B]. https://doi.org/10.1039/D4SC03926B

Vancouver

Szlosek R, Marquardt C, Hegen O, Balazs G, Riesinger C, Тимошкин АЮ и пр. Synthesis of bismuthanyl-substituted monomeric triel hydrides. Chemical Science. 2024 Авг. 12;15(36):14837-14843. D4SC03926B. https://doi.org/10.1039/D4SC03926B

Author

Szlosek, Robert ; Marquardt, Christian ; Hegen, Oliver ; Balazs, Gabor ; Riesinger, Christoph ; Тимошкин, Алексей Юрьевич ; Scheer, M. / Synthesis of bismuthanyl-substituted monomeric triel hydrides. в: Chemical Science. 2024 ; Том 15, № 36. стр. 14837-14843.

BibTeX

@article{ac27aa9a434941b296c26133984ee154,
title = "Synthesis of bismuthanyl-substituted monomeric triel hydrides",
abstract = "The syntheses and characterizations of the first bismuthanylborane monomers stabilized only by a donor in D$BH2Bi(SiMe3)2 (D = DMAP 1a, IDipp 1b, IMe4 1c; DMAP = 4-dimethylaminopyridine, IDipp = 1,3-bis(2,6diisopropylphenyl)-imidazolin-2-ylidene, IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene) are presented. All compounds were synthesized by salt metathesis reactions between D$BH2I and KBi(SiMe3)2(THF)0.3 and represent some of the extremely rare compounds featuring a 2c–2e B–Bi bond in a molecular compound. The products display high sensitivity towards air and light and slowly decompose in solution even at −80 °C. By the reaction of IDipp$GaH2(SO3CF3) with KBi(SiMe3)2(THF)0.3, the synthesis of the first bismuthanylgallane IDipp$GaH2Bi(SiMe3)2 (2) stabilized only by a 2-electron donor was possible, as evident from single crystal X-ray structure determination, NMR spectroscopy and mass spectrometry. Computational studies shed light on the stability of the products and the electronic nature of the compounds.",
author = "Robert Szlosek and Christian Marquardt and Oliver Hegen and Gabor Balazs and Christoph Riesinger and Тимошкин, {Алексей Юрьевич} and M. Scheer",
year = "2024",
month = aug,
day = "12",
doi = "10.1039/D4SC03926B",
language = "English",
volume = "15",
pages = "14837--14843",
journal = "Chemical Science",
issn = "2041-6520",
publisher = "Royal Society of Chemistry",
number = "36",

}

RIS

TY - JOUR

T1 - Synthesis of bismuthanyl-substituted monomeric triel hydrides

AU - Szlosek, Robert

AU - Marquardt, Christian

AU - Hegen, Oliver

AU - Balazs, Gabor

AU - Riesinger, Christoph

AU - Тимошкин, Алексей Юрьевич

AU - Scheer, M.

PY - 2024/8/12

Y1 - 2024/8/12

N2 - The syntheses and characterizations of the first bismuthanylborane monomers stabilized only by a donor in D$BH2Bi(SiMe3)2 (D = DMAP 1a, IDipp 1b, IMe4 1c; DMAP = 4-dimethylaminopyridine, IDipp = 1,3-bis(2,6diisopropylphenyl)-imidazolin-2-ylidene, IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene) are presented. All compounds were synthesized by salt metathesis reactions between D$BH2I and KBi(SiMe3)2(THF)0.3 and represent some of the extremely rare compounds featuring a 2c–2e B–Bi bond in a molecular compound. The products display high sensitivity towards air and light and slowly decompose in solution even at −80 °C. By the reaction of IDipp$GaH2(SO3CF3) with KBi(SiMe3)2(THF)0.3, the synthesis of the first bismuthanylgallane IDipp$GaH2Bi(SiMe3)2 (2) stabilized only by a 2-electron donor was possible, as evident from single crystal X-ray structure determination, NMR spectroscopy and mass spectrometry. Computational studies shed light on the stability of the products and the electronic nature of the compounds.

AB - The syntheses and characterizations of the first bismuthanylborane monomers stabilized only by a donor in D$BH2Bi(SiMe3)2 (D = DMAP 1a, IDipp 1b, IMe4 1c; DMAP = 4-dimethylaminopyridine, IDipp = 1,3-bis(2,6diisopropylphenyl)-imidazolin-2-ylidene, IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene) are presented. All compounds were synthesized by salt metathesis reactions between D$BH2I and KBi(SiMe3)2(THF)0.3 and represent some of the extremely rare compounds featuring a 2c–2e B–Bi bond in a molecular compound. The products display high sensitivity towards air and light and slowly decompose in solution even at −80 °C. By the reaction of IDipp$GaH2(SO3CF3) with KBi(SiMe3)2(THF)0.3, the synthesis of the first bismuthanylgallane IDipp$GaH2Bi(SiMe3)2 (2) stabilized only by a 2-electron donor was possible, as evident from single crystal X-ray structure determination, NMR spectroscopy and mass spectrometry. Computational studies shed light on the stability of the products and the electronic nature of the compounds.

UR - https://www.mendeley.com/catalogue/a957d231-bf25-375e-a16d-a322b8c3ef1e/

U2 - 10.1039/D4SC03926B

DO - 10.1039/D4SC03926B

M3 - Article

C2 - 39184294

VL - 15

SP - 14837

EP - 14843

JO - Chemical Science

JF - Chemical Science

SN - 2041-6520

IS - 36

M1 - D4SC03926B

ER -

ID: 123909839