首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Spectroscopic and Luminescence Studies on Square-Planar Platinum(II) Complexes with Anionic Tridentate 3-Bis(2-pyridylimino)isoindoline Derivatives
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Spectroscopic and Luminescence Studies on Square-Planar Platinum(II) Complexes with Anionic Tridentate 3-Bis(2-pyridylimino)isoindoline Derivatives

机译:阴离子-三齿3-双(2-吡啶基氨基)异吲哚啉衍生物的方形-平面铂(II)配合物的光谱和发光研究

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摘要

Reactions of 1,3-bis(2-pyridylimino)isoindoline (HL1), 1,3-bis(2-pyridylimino)benz(f)isoindoline (HL2), or 5,6-dihydro-2,3-diphenyl-5-(pyridin-2-ylimino)pyrrolo[3,4-b]pyrazin-7-yl idene)pyridin-2-amine (HL3) with Pt(tht)(2)Cl-2 (tht = tetrahydrothiophene) afforded the corresponding Pt(L)Cl complexes. A series of neutral platinum(II) alkynyl complexes Pt(L)(C CR) were prepared by reactions of the precursors Pt(L)Cl with alkynyl ligands through Cul-catalyzed platinum acetylide sigma coordination. Crystal structural determination of Pt(L3)Cl (3), Pt(L1)(C CPh) (4), and Pt(L1)(C CC6H4But-4) (6) by X-ray crystallography revealed that the neutral platinum(Pi) complexes with monoanionic tridentate L ligands display more perfect square-planar geometry than that in platinum(II) complexes with neutral tridentate 2,2':6,2 ''-terpyridyl ligands. Both the Pt(L)Cl and Pt(L)(C CC6H4R-4) complexes exhibit low-energy absorption at 400-550 nm, arising primarily from pi -> pi*(L) intraligand (IL) and 5d(Pt) -> pi*(L) metal-to-ligand charge-transfer (MLCT) transitions as suggested from density functional theory calculations. They display bright-orange to red room-temperature luminescence in fluid dichloromethane solutions with microsecond to submicrosecond ranges of emissive lifetimes and 0.03-3.79% quantum yields, originating mainly from (IL)-I-3 and (MLCT)-M-3 excited states. Compared with the emissive state in Pt(L)Cl complexes, substitution of the coordinated Cl with C CC6H4R-4 in Pt(L)(C CC6H4R-4) complexes induces an obviously enhanced contribution from the (3)[pi-(C CC6H4R-4) -> pi*(L)] ligand-to-ligand charge-transfer (LLCT) triplet state. The photophysical properties can be finely tuned by modifying both the L and alkynyl ligands. The calculated absorption and emission spectra in dichloromethane coincide well with those measured in a fluid dichloromethane solution at ambient temperature.
机译:1,3-双(2-吡啶基氨基)异吲哚啉(HL1),1,3-双(2-吡啶基氨基)苯(f)异吲哚啉(HL2)或5,6-二氢-2,3-二苯基-5的反应-与(Pt(tht)(2)Cl-2(tht =四氢噻吩)的-(吡啶-2-吡啶基)吡咯并[3,4-b]吡嗪-7-基烯基)吡啶-2-胺(HL3)得到相应的Pt(L)Cl络合物。通过前驱体Pt(L)Cl与炔基配体的反应,通过Cul催化的铂乙炔sigma配位反应,制备了一系列中性的铂(II)炔基络合物Pt(L)(C CR)。通过X射线晶体学测定Pt(L3)Cl(3),Pt(L1)(C CPh)(4)和Pt(L1)(C CC6H4But-4)(6)的晶体结构表明,中性铂(具有单阴离子三齿L配体的Pi)配合物比具有中性三齿2,2':6,2''-吡啶基配体的铂(II)配合物显示出更完美的正方形平面几何形状。 Pt(L)Cl和Pt(L)(C CC6H4R-4)络合物在400-550 nm处均显示出低能量吸收,主要是由于pi-> pi *(L)内配体(IL)和5d(Pt) -> pi *(L)金属到配体的电荷转移(MLCT)跃迁,这是根据密度泛函理论计算得出的。它们在液态二氯甲烷溶液中显示亮橙色至红色的室温发光,其发射寿命为微秒至亚微秒范围,且量子产率为0.03-3.79%,主要来自(IL)-I-3和(MLCT)-M-3激发状态。与Pt(L)Cl络合物的发射态相比,Pt(L)(C CC6H4R-4)络合物中的C CC6H4R-4取代配位Cl引起(3)[pi-(C CC6H4R-4)-> pi *(L)]配体到配体的电荷转移(LLCT)三重态。可以通过同时修饰L和炔基配体来微调光物理性质。在二氯甲烷中计算的吸收光谱和发射光谱与在室温下在流体二氯甲烷溶液中测得的光谱非常吻合。

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