2011
DOI: 10.1016/j.saa.2011.04.067
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A phosphorescent copper(I) complex: Synthesis, characterization, photophysical property, and oxygen-sensing behavior

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Cited by 27 publications
(12 citation statements)
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“…357,358 The crystals can be excited in the near-UV at B375 nm to emit yellow-green luminescence with a maximum at 540 nm. Another phosphorescent copper(I) complex 359 with an RTP phosphorescence peaking at 545 nm and a long excited state lifetime (4.7 ms) was incorporated into electrospun composite nanofibers of polystyrene to obtain an oxygen sensing material with a sensitivity (I 0 /I 100 ) of 7.2 and a response time of 7 s. No photobleaching was detectable. The exceptionally long-lived luminescence of certain [Cu(I)(isocyanido) 2 (phen)] + complexes in the form of nanoporous crystals may also be exploited for sensing oxygen.…”
Section: Metalloporphyrins With Large Q-band Absorption and Nir Emissmentioning
confidence: 99%
“…357,358 The crystals can be excited in the near-UV at B375 nm to emit yellow-green luminescence with a maximum at 540 nm. Another phosphorescent copper(I) complex 359 with an RTP phosphorescence peaking at 545 nm and a long excited state lifetime (4.7 ms) was incorporated into electrospun composite nanofibers of polystyrene to obtain an oxygen sensing material with a sensitivity (I 0 /I 100 ) of 7.2 and a response time of 7 s. No photobleaching was detectable. The exceptionally long-lived luminescence of certain [Cu(I)(isocyanido) 2 (phen)] + complexes in the form of nanoporous crystals may also be exploited for sensing oxygen.…”
Section: Metalloporphyrins With Large Q-band Absorption and Nir Emissmentioning
confidence: 99%
“…They are essentially metal-based orbitals with some contribution of the styryl ligand for diimine complexes (C3, C4 and C5), whereas they are delocalized over the metal and phosphines for complexes with DPEphos (C1 and C2), in agreement with literature data. [53][54][55] Besides, the energy spacing between HOMO-1 and HOMO-2 is larger for bisphosphine complexes while it is weaker in bisdiimine complexes. On the other hand, the LUMO and LUMO+1 are localized on the pyridyl moieties of styryl bipyridine for mixed [Cu(P^P)(N^N)]PF 6 complexes, while in bisdiimine complexes the LUMO+1 is fully localized on L1 and its energy is close to the LUMO (fully residing on the styryl bipyridine).…”
Section: Computational Studymentioning
confidence: 99%
“…During the last decade, phosphorescent Cu(I) complexes have gained increasing interest for their potential applications in organic light emitting diodes (OLEDs), [1][2][3][4][5][6] light emitting electrochemical cells (LEECs), [7][8] chemosensor [9][10][11][12][13] and photocatalysts. [14][15][16][17][18] One of the most important reason is that Cu(I) complexes are low-cost, high-abundant and environmentally benign, compared to Ru(II), Ir(III) and Pt(II) metal complexes.…”
Section: Introductionmentioning
confidence: 99%