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Synthesis, characterization and electrochemiluminescent properties of cyclometalated platinum(II) complexes with substituted 2-phenylpyridine ligands

Two neutral cyclometalated platinum(II) complexes, Pt(DPP)(acac) and Pt(BPP)(acac) (DPP = 2,4-diphenylpyridine, BPP = 2-(4-tert-butylphenyl)-4-phenylpyridine, acac = acetylacetone), have been synthesized and characterized by (1)H NMR spectroscopy, mass spectrometry, elemental analyses and by X-ray c...

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Published in:Dalton transactions : an international journal of inorganic chemistry 2013-03, Vol.42 (11), p.4059-4067
Main Authors: Li, Chunxiang, Wang, Shuqin, Huang, Yangmei, Zheng, Bin, Tian, Ziqi, Wen, Yonghong, Li, Feng
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container_title Dalton transactions : an international journal of inorganic chemistry
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Wang, Shuqin
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Wen, Yonghong
Li, Feng
description Two neutral cyclometalated platinum(II) complexes, Pt(DPP)(acac) and Pt(BPP)(acac) (DPP = 2,4-diphenylpyridine, BPP = 2-(4-tert-butylphenyl)-4-phenylpyridine, acac = acetylacetone), have been synthesized and characterized by (1)H NMR spectroscopy, mass spectrometry, elemental analyses and by X-ray crystallography for Pt(DPP)(acac). Electrogenerated chemiluminescence (ECL) of the two complexes in the absence or presence of coreactant tri-n-propylamine (TPrA) in different solvents (CH(3)CN, CH(2)Cl(2), DMF, CH(3)CN/H(2)O (V, 50 : 50)) has been studied. The ECL spectra are identical to their own PL spectra, indicating that ECL processes lead to the same metal-to-ligand charge-transfer ((3)MLCT) excited state that is generated by light excitation. The ECL potentials of Pt(DPP)(acac) and Pt(BPP)(acac)/TPrA in CH(3)CN and CH(3)CN/H(2)O solution were at ~0.75 V vs. SCE, and significantly negatively shifted by about 0.6 V compared to that of the Ru(bpy)(3)(2+)/TPrA system. The ECL quantum efficiencies of the complexes are comparable to that of the Ru(bpy)(3)(2+)/TPrA system. The significant increase of the ECL signal in the coreactant system is due to the formation of the strongly reducing intermediate TPrA˙. It is noteworthy that the ECL efficiencies of the synthesized compounds are much higher than that of the tridentate polypyridyl ligands.
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Electrogenerated chemiluminescence (ECL) of the two complexes in the absence or presence of coreactant tri-n-propylamine (TPrA) in different solvents (CH(3)CN, CH(2)Cl(2), DMF, CH(3)CN/H(2)O (V, 50 : 50)) has been studied. The ECL spectra are identical to their own PL spectra, indicating that ECL processes lead to the same metal-to-ligand charge-transfer ((3)MLCT) excited state that is generated by light excitation. The ECL potentials of Pt(DPP)(acac) and Pt(BPP)(acac)/TPrA in CH(3)CN and CH(3)CN/H(2)O solution were at ~0.75 V vs. SCE, and significantly negatively shifted by about 0.6 V compared to that of the Ru(bpy)(3)(2+)/TPrA system. The ECL quantum efficiencies of the complexes are comparable to that of the Ru(bpy)(3)(2+)/TPrA system. The significant increase of the ECL signal in the coreactant system is due to the formation of the strongly reducing intermediate TPrA˙. 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It is noteworthy that the ECL efficiencies of the synthesized compounds are much higher than that of the tridentate polypyridyl ligands.</description><subject>Acetylacetone</subject><subject>Chemiluminescence</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - chemistry</subject><subject>Crystallography, X-Ray</subject><subject>Electrochemistry</subject><subject>Excitation spectra</subject><subject>Lead (metal)</subject><subject>Ligands</subject><subject>Luminescence</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mass Spectrometry</subject><subject>Models, Molecular</subject><subject>Molecular Dynamics Simulation</subject><subject>NMR spectroscopy</subject><subject>Organoplatinum Compounds - chemical synthesis</subject><subject>Organoplatinum Compounds - chemistry</subject><subject>Pyridines - chemical synthesis</subject><subject>Pyridines - chemistry</subject><subject>Solvents</subject><subject>Spectra</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0U1PFTEUBuCGaACBjT_AdAnGkX5M29slIag3IXGhrCed9tQpdD5sO5Hxf_h_HXKvuNTVOYsn78nJi9BrSt5TwvWlZa5wVkv5cICOaa1UpRmvXzzvTB6hVznfE8IYEewQHTHOa6K0PEa_vixD6SCH_A7bziRjC6Tw05QwDtgMDkMEW9JoO-hDnPswQLYwFDylcYJUAmQ8emwXG8ceiommgMPTOsIw9-fb7QW2Yz9FeFzhj1A6nOc2l1DmJ8eqqYNhidOSglujcQzf1qP5FL30JmY4288TdPfh5uv1p-r288ft9dVtZbngpTJWOK9bKTTxrRAbT33rJHjNwErmOGPCypoSopxvJZNEMi5a7msnraHa8BN0vstdv_k-Qy5NH9b3YjQDjHNuqOKE6Fps1L9pTdVGKSH_gzJNhd4orVf6dkdtGnNO4Jsphd6kpaGkeSq3-Vvuit_sc-e2B_dM_7TJfwPv06QS</recordid><startdate>20130321</startdate><enddate>20130321</enddate><creator>Li, Chunxiang</creator><creator>Wang, Shuqin</creator><creator>Huang, Yangmei</creator><creator>Zheng, Bin</creator><creator>Tian, Ziqi</creator><creator>Wen, Yonghong</creator><creator>Li, Feng</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7SR</scope><scope>8BQ</scope><scope>JG9</scope></search><sort><creationdate>20130321</creationdate><title>Synthesis, characterization and electrochemiluminescent properties of cyclometalated platinum(II) complexes with substituted 2-phenylpyridine ligands</title><author>Li, Chunxiang ; 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Electrogenerated chemiluminescence (ECL) of the two complexes in the absence or presence of coreactant tri-n-propylamine (TPrA) in different solvents (CH(3)CN, CH(2)Cl(2), DMF, CH(3)CN/H(2)O (V, 50 : 50)) has been studied. The ECL spectra are identical to their own PL spectra, indicating that ECL processes lead to the same metal-to-ligand charge-transfer ((3)MLCT) excited state that is generated by light excitation. The ECL potentials of Pt(DPP)(acac) and Pt(BPP)(acac)/TPrA in CH(3)CN and CH(3)CN/H(2)O solution were at ~0.75 V vs. SCE, and significantly negatively shifted by about 0.6 V compared to that of the Ru(bpy)(3)(2+)/TPrA system. The ECL quantum efficiencies of the complexes are comparable to that of the Ru(bpy)(3)(2+)/TPrA system. The significant increase of the ECL signal in the coreactant system is due to the formation of the strongly reducing intermediate TPrA˙. It is noteworthy that the ECL efficiencies of the synthesized compounds are much higher than that of the tridentate polypyridyl ligands.</abstract><cop>England</cop><pmid>23340796</pmid><doi>10.1039/c2dt32466k</doi><tpages>9</tpages></addata></record>
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1477-9234
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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Acetylacetone
Chemiluminescence
Coordination Complexes - chemical synthesis
Coordination Complexes - chemistry
Crystallography, X-Ray
Electrochemistry
Excitation spectra
Lead (metal)
Ligands
Luminescence
Magnetic Resonance Spectroscopy
Mass Spectrometry
Models, Molecular
Molecular Dynamics Simulation
NMR spectroscopy
Organoplatinum Compounds - chemical synthesis
Organoplatinum Compounds - chemistry
Pyridines - chemical synthesis
Pyridines - chemistry
Solvents
Spectra
title Synthesis, characterization and electrochemiluminescent properties of cyclometalated platinum(II) complexes with substituted 2-phenylpyridine ligands
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