Syntheses, structures, and solid-state phosphorescence characteristics of trans-bis(salicylaldiminato)Pt(II) complexes bearing perpendicular N-aryl functionalities
Syntheses, structures, and solid-state phosphorescence characteristics of trans-bis(salicylaldiminato)Pt(II) complexes bearing perpendicular N-aryl functionalities
复制标题
具有垂直N-芳基官能团的反式双(水杨醛亚胺)Pt(II)配合物的合成、结构和固态磷光特性
DOI:
10.1007/s11243-017-0198-9
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发表时间:
2017
影响因子:
1.7
通讯作者:
Naota Takeshi
中科院分区:
文献类型:
--
作者:
Iwata Shotaro;Takahashi Hidenori;Ihara Asami;Hiramatsu Kumiko;Adachi Junya;Kawamorita Soichiro;Komiya Naruyoshi;Naota Takeshi
The syntheses, structures, and solid-state emission characteristics oftrans-bis(salicylaldiminato)Pt(II) complexes bearingN-aromatic functionalities are described herein. A series of Pt complexes bearing variousN-phenyl (1) andN-(1-naphthyl) (2) groups on the salicylaldiminato ligands were prepared by reacting PtCl2(CH3CN)2with the correspondingN-salicylidene aromatic amines, and thetrans-coordination and crystal packing of these complexes were unequivocally established based on X-ray diffraction (XRD). Complexes with 2,6-dimethylphenyl (1c), 2,6-diisopropylphenyl (1d), 1-naphthyl (2a), and 1-(2-methylnaphthyl) (2b) groups on the N atoms exhibited intense phosphorescent emission at ambient temperature in the crystalline state, while those with phenyl (1a), 2,6-dibromophenyl (1b), and 2,6-bis(N,N-dimethylamino)phenyl (1e) functionalities were either less emissive or non-emissive under the same conditions. XRD analyses identified significant intramolecular interactions between Pt and H atoms of theN-aryl functionalities in the emissive crystals of1c,1d, and2a. These interactions were evidently an important factor associated with intense emission at ambient temperature.