کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1335024 1500224 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis and characterization of phosphorescent cyclometalated Ir and Pt heteroleptic complexes using cyclophane-based chelates
ترجمه فارسی عنوان
سنتز و مشخصه های مجتمع های هترولوپتیک ایر و پت فسفرسنت سیکلومتال شده با استفاده از کلات های مبتنی بر سیکلوفان
کلمات کلیدی
فسفر رزونانس، ایریدیوم، پلاتین، لومینسنت، سیکلوفن
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی

The synthesis and characterization of a series of neutral cyclometalated Pt(II) and Ir(III) heteroleptic complexes containing cyclophane substituted chelates is reported. The complexes have the general formula of (C^N)Pt(O^O) or (C^N)2Ir(O^O) where C^N is a monoanionic cyclophane ligand 2-([2.2]-paracyclophane-4-yl)pyridyl (pCpy) or 1-([2.2]-paracyclophane-4-yl)pyrazolyl (pCpz) and (O^O) is an ancillary ligand; acetylacetonato (acac) or dipivolylmethanato (dpm). The pCpyH and pCpzH ligand precursors were obtained as racemates due to the planar chirality of the cyclophane ring system. Two diastereomers of (pCpz)2Ir(acac), one with C1 symmetry (ΛRS, ΔSR) and the other with C2 symmetry (ΛRR, ΔSS) were isolated, whereas only one C1 diastereomer was obtained for (pCpy)2Ir(acac). Inherent strain in the cyclophane core and transannular interaction between the bridged phenyl rings leads to a 250–400 mV cathodic shift in the oxidation potentials relative to analogous complexes with ppy or ppz ligands. The destabilization of the HOMO leads to a corresponding red shift in the absorption and emission spectra from the complexes with pCpy and pCpz ligands. The Pt and Ir complexes with pCpy ligands are strongly emissive at room temperature, whereas complexes with pCpz ligands are only weakly emissive as they still suffer from temperature-dependent nonradiative deactivation to metal-centered ligand field states.

The synthesis and characterization of a series of neutral cyclometalated Pt(II) and Ir(III) heteroleptic complexes containing cyclophane substituted chelates is reported. The complexes have the general formula of (C^N)Pt(O^O) or (C^N)2Ir(O^O) where C^N is a monoanionic cyclophane ligand 2-([2.2]-paracyclophane-4-yl)pyridyl (pCpy) or 1-([2.2]-paracyclophane-4-yl)pyrazolyl (pCpz) and (O^O) is an ancillary ligand; acetylacetonato (acac) or dipivolylmethanato (dpm).Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Polyhedron - Volume 116, 25 September 2016, Pages 182–188
نویسندگان
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