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Synthesis, crystal structure and luminescent properties of novel lanthanide complexes with CAPh type ligand diphenyl-N-benzoylamidophosphate and bidentate nitrogen donors
Herein we report the synthesis and investigations of the new lanthanide coordination compounds [LnL3bipy] (Ln1) and [LnL3phen] (Ln2) with carbacylamidophosphate type ligand diphenyl-N-benzoylamidophosphate (HL = [PhCONHPO(OPh)2]) and additional ligands 2,2′-bipyridine and 1,10-phenantroline. The obt...
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Published in: | Journal of luminescence 2020-07, Vol.223, p.117187, Article 117187 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Herein we report the synthesis and investigations of the new lanthanide coordination compounds [LnL3bipy] (Ln1) and [LnL3phen] (Ln2) with carbacylamidophosphate type ligand diphenyl-N-benzoylamidophosphate (HL = [PhCONHPO(OPh)2]) and additional ligands 2,2′-bipyridine and 1,10-phenantroline. The obtained complexes were characterized by means of X-Ray, thermal gravimetric analysis, IR, 1H NMR, UV absorption spectroscopy and luminescence spectroscopy at 298 and 77 K. The X-ray diffraction analysis of Eu1 and Eu2 shows that the complexes crystalize in monoclinic crystal system, P 21/n space group. Efficient energy transfer from organic ligands after their excitation sensitizes the lanthanide interior emission from 5D0 or 5D4 levels of EuIII or TbIII respectively, leading to a strong metal-centered luminescence with decay time 1.5–2.0 ms. Intrinsic quantum yields (QLnLn) for europium complexes found to be equal 78 (Eu1) and 70% (Eu2). Overall QY equals 46 and 42% respectively.
•The novel CAPh based lanthanide complexes LnL3bipy and LnL3phen were synthesized.•The europium complexes crystal structure was solved.•The complexes were found to be stable till over 200 °C.•EuIII and TbIII complexes exhibit strong rather long-lived metal centered emission in solid and in solution. |
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ISSN: | 0022-2313 1872-7883 |
DOI: | 10.1016/j.jlumin.2020.117187 |