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Solid State Phosphorescence Enhancement of PtII-Based Emitters Via Combination of π-Hole(Isocyano Group)⋅⋅⋅ dz2[PtII] and I···Cl Halogen-Bonding Interactions. / Katkova, Svetlana A.; Antonova, Elina V.; Cheranyova, Anna M.; Ivanov, Daniil M.; Kinzhalov, Mikhail A.
в: Inorganics, Том 11, № 10, 403, 13.10.2023.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Solid State Phosphorescence Enhancement of PtII-Based Emitters Via Combination of π-Hole(Isocyano Group)⋅⋅⋅ dz2[PtII] and I···Cl Halogen-Bonding Interactions
AU - Katkova, Svetlana A.
AU - Antonova, Elina V.
AU - Cheranyova, Anna M.
AU - Ivanov, Daniil M.
AU - Kinzhalov, Mikhail A.
PY - 2023/10/13
Y1 - 2023/10/13
N2 - The PtII isocyanide complex [Pt(ppy)Cl(CNC6H4-C≡C-Ph)] (1, Hppy=2-phenylpyridine) was co-crystallized with 1,4-diiodotetrafluorobenzene (1,4-DITFB), yielding 1·½(1,4-DITFB) adduct. The I···Cl halogen-bonding and π-π-stacking interactions combined with the rare π-hole(isocyano group)⋅⋅⋅dz2[PtII] interactions were identified via analysis of X-ray diffraction data of the co-crystals. These two types of structure-determining interactions supplemented each other, and the system of I⋯Cl and π-hole(isocyano group)⋅⋅⋅dz2[PtII] contacts achieved a 1D extended ladder-type architecture. The density functional theory calculations, employing a set of computational tools, verified the role of I⋯Cl and π-hole(isocyano group)⋅⋅⋅dz2[PtII] noncovalent bonds in the spectrum of noncovalent forces. The solid-state photophysical study revealed an amplification of luminescence intensity in the co-crystals, which is attributed to the suppression of the nonradiative relaxation pathways due to an increase in the rigidity of the chromophore center.
AB - The PtII isocyanide complex [Pt(ppy)Cl(CNC6H4-C≡C-Ph)] (1, Hppy=2-phenylpyridine) was co-crystallized with 1,4-diiodotetrafluorobenzene (1,4-DITFB), yielding 1·½(1,4-DITFB) adduct. The I···Cl halogen-bonding and π-π-stacking interactions combined with the rare π-hole(isocyano group)⋅⋅⋅dz2[PtII] interactions were identified via analysis of X-ray diffraction data of the co-crystals. These two types of structure-determining interactions supplemented each other, and the system of I⋯Cl and π-hole(isocyano group)⋅⋅⋅dz2[PtII] contacts achieved a 1D extended ladder-type architecture. The density functional theory calculations, employing a set of computational tools, verified the role of I⋯Cl and π-hole(isocyano group)⋅⋅⋅dz2[PtII] noncovalent bonds in the spectrum of noncovalent forces. The solid-state photophysical study revealed an amplification of luminescence intensity in the co-crystals, which is attributed to the suppression of the nonradiative relaxation pathways due to an increase in the rigidity of the chromophore center.
KW - halogen bonding
KW - isocyanide ligands
KW - luminescence
KW - noncovalent interactions
KW - platinum(II) complexes
KW - π-hole interactions
UR - https://www.mendeley.com/catalogue/7ba9ae28-2fdb-35d4-bb61-2c9b1e371e27/
U2 - 10.3390/inorganics11100403
DO - 10.3390/inorganics11100403
M3 - Article
VL - 11
JO - Inorganics
JF - Inorganics
SN - 2304-6740
IS - 10
M1 - 403
ER -
ID: 111607003