Electronic spectroscopy, photophysical properties, and emission quenching studies of an oxidatively robust perfluorinated platinum porphyrin

• Published in: Inorganic Chemistry
• Main Authors: Lai, SW, Hou, YJ, Che, CM, Pang, HL, Wong, KY, Chang, CK, Zhu, NY
• Format: Article in Journal/Newspaper
• Language: English
• Published: 2004
• Subjects: DML
• Online Access: http://repository.ust.hk/ir/Record/1783.1-21586; https://doi.org/10.1021/ic049902h; http://lbdiscover.ust.hk/uresolver?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rfr_id=info:sid/HKUST:SPI&rft.genre=article&rft.issn=0020-1669&rft.volume=43&rft.issue=12&rft.date=2004&rft.spage=3724&rft.epage=3732&rft.aulast=Lai&rft.aufirst=SW&rft.atitle=Electronic+spectroscopy,+photophysical+properties,+and+emission+quenching+studies+of+an+oxidatively+robust+perfluorinated+platinum+porphyrin; http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=LinksAMR&SrcApp=PARTNER_APP&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000221989000025; http://www.scopus.com/record/display.url?eid=2-s2.0-2942605723&origin=inward

The highly electron-deficient, beta-octafluorinated meso-tetrakis(pentafluorophenyl)-porphyrin (H2F28TPP) was metalated with platinum to afford the oxidatively robust luminophore [PtF28TPP], and its X-ray structure shows that the porphyrin core exists in a slightly saddle-shaped conformation. The absorption spectrum of [PtF28TPP] in CH2Cl2 displays a near-UV Soret band (B) at 383 nm (epsilon = 2.85 x 10(5) dm(3) mol(-1) cm(-1)) and two visible 0(1,0) and Q(0,0) bands at 501 (epsilon = 1.45 x 10(4) dm(3) Mol(-1) cm(-1)) and 533 (6 = 1.36 x 10(4) dml mol(-1) cm(-1)) nm, respectively. These absorption bands of [PtF28TPP] are blue-shifted from those in [PtF20TPP] (390, 504, and 538 nm, respectively) and [PtTPP] (401, 509, and 539 nm, respectively). Excitation of [PtF28TPP] (complex concentration = 1.5 x 10(-6) Mol dm(-3)) in dichloromethane at the Soret or Q(1,0) or Q(0,0) band gave a phosphorescence with peak maximum at 650 nm (lifetime = 5.8 mus) and a weak shoulder at 712 nm. Both the emission lifetime and quantum yield vary with solvent polarity, and plots of tau versus E-K and Phi versus E-K (where EK is the empirical solvent polarity parameter based on the hypsochromic shift of the longest wavelength absorption of the [Mo(CO)(4){(C5H4N)HC=NCH2C6H5}] complex with increasing solvent polarity; see: Kamlet, M. J.; Abboud, J. L. M.; Taft, R. W. Prog. Phys. Org. Chem, 1981, 13, pp 485-630) show linear correlation, indicating that the emission is sensitive to the local environment/medium, Electrochemical studies on [PtF28TPP] by cyclic voltammetry showed no porphyrin-centered oxidation at potential less than or equal to 1.5 V versus Ag/AgNO3, demonstrating that [PtF28TPP] is more resistant toward oxidation than [PtF20-TPP] (E-1/2 = 1.33 V) and [PtTPP] (E-1/2 = 0.97 V). The porphyrin-centered reduction of [PtF28TPP] occurs at -0.75 and -1.18 V, which is anodically shifted from those at -1.06 and -1.55 V in [PtF20TPP], and -1.51 V in [PtTPP], respectively. The excited-state reduction potential of [PtF28TPP] is estimated to be 1.49 V versus Ag/AgNO3. Over 97\% of the emission intensity of [PtF28TPP] was retained after irradiation with a high power mercury arc lamp (500 W) for 14 h, compared to 90\% and 12\% for [PtF20TPP] and [PtTPP], respectively; hence, [PtF28TPP] exhibits superior photostability. Quenching of the emission of [PtF28TPP] by oxygen, alcohol, catechol, and butylamine reveals that [PtF28TPP] is an oxidatively robust material with medium-sensitive photoluminescence properties.