TY - JOUR
T1 - Dinuclear fused salen complexes of group-10 metals
T2 - Peculiarity of the crystal structure and near-infrared luminescence of a bis(Pt-salen) complex
AU - Houjou, Hirohiko
AU - Hoga, Yuki
AU - Ma, Yi Lan
AU - Achira, Hiroto
AU - Yoshikawa, Isao
AU - Mutai, Toshiki
AU - Matsumura, Kazunari
N1 - Funding Information:
A part of this work (X-ray single crystallographic structure analysis) was carried out at the Research Hub for Advanced Nano Characterization, University of Tokyo, and was supported by the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan. T. Mutai gratefully acknowledges the financial support from the Japan Society for the Promotion of Science (Grants-in-Aid for Scientific Research C 16K05743).
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017
Y1 - 2017
N2 - Dinuclear fused salen complexes with Ni, Pd, and Pt nuclei were synthesized, and their crystal structures were determined. In the crystal structure of the Pt complexes, the molecules were virtually planar and formed a closely stacked dimer every two molecules, whose Pt—Pt interatomic distance was 3.43 Å. The absorption spectra of the dinuclear salen complexes were similar to each other both in solution and in the solid state. The dinuclear Pt complex exhibited photoluminescence, presumably related to the π-conjugated system of the naphthalene ring, both in solution and in the solid state. The low-energy emission, corresponding to a longer wavelength compared to that of analogous mononuclear complexes, ranged to the near-infrared region, suggesting that the naphthalene ring is perturbed by the adjoining chelate rings as if these moieties formed a fused aromatic ring system.
AB - Dinuclear fused salen complexes with Ni, Pd, and Pt nuclei were synthesized, and their crystal structures were determined. In the crystal structure of the Pt complexes, the molecules were virtually planar and formed a closely stacked dimer every two molecules, whose Pt—Pt interatomic distance was 3.43 Å. The absorption spectra of the dinuclear salen complexes were similar to each other both in solution and in the solid state. The dinuclear Pt complex exhibited photoluminescence, presumably related to the π-conjugated system of the naphthalene ring, both in solution and in the solid state. The low-energy emission, corresponding to a longer wavelength compared to that of analogous mononuclear complexes, ranged to the near-infrared region, suggesting that the naphthalene ring is perturbed by the adjoining chelate rings as if these moieties formed a fused aromatic ring system.
KW - Metal-metal contact
KW - Near-infrared emission
KW - Photoluminescence
KW - Quasi aromaticity
KW - π-Conjugated system
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U2 - 10.1016/j.ica.2017.01.031
DO - 10.1016/j.ica.2017.01.031
M3 - Article
AN - SCOPUS:85013020859
SN - 0020-1693
VL - 461
SP - 27
EP - 34
JO - Inorganica Chimica Acta
JF - Inorganica Chimica Acta
ER -