Photophysics of Cage/Guest Assemblies: Photoinduced Electron Transfer between a Coordination Cage Containing Osmium(II) Luminophores, and Electron-Deficient Bound Guests in the Central Cavity

A heterometallic octanuclear coordination cage [Os4Zn4(Lnap)12]­X16 (denoted Os•Zn; X = perchlorate or chloride) has been prepared (Lnap is a bis-bidentate bridging ligand containing two pyrazolyl–pyridine chelating units separated by a 1,5-naphthalenediyl spacer group). The {Os­(NN)3}2+ units locat...

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Veröffentlicht in:Inorganic chemistry 2019-02, Vol.58 (4), p.2386-2396
Hauptverfasser: Train, Jennifer S, Wragg, Ashley B, Auty, Alexander J, Metherell, Alexander J, Chekulaev, Dimitri, Taylor, Christopher G. P, Argent, Stephen P, Weinstein, Julia A, Ward, Michael D
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Sprache:eng
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Zusammenfassung:A heterometallic octanuclear coordination cage [Os4Zn4(Lnap)12]­X16 (denoted Os•Zn; X = perchlorate or chloride) has been prepared (Lnap is a bis-bidentate bridging ligand containing two pyrazolyl–pyridine chelating units separated by a 1,5-naphthalenediyl spacer group). The {Os­(NN)3}2+ units located at four of the eight vertices of the cube have a long-lived, phosphorescent 3MLCT excited state which is a stronger electron donor than [Ru­(bipy)3]2+. The chloride form of Os•Zn is water-soluble and binds in its central cavity the hydrophobic electron-accepting organic guests 1,2,4,5-tetracyanobenzene, 1,4-naphthoquinone and 1-nitronaphthalene, with binding constants in the range 103–104 M–1, resulting in quenching of the phosphorescence arising from the Os­(II) units. A crystal structure of an isostructural Co8 cage containing one molecule of 1,2,4,5-tetracyanobenzene as a guest inside the cavity has been determined. Ultrafast transient absorption measurements show formation of a charge-separated Os­(III)/guest•– state arising from cage-to-guest photoinduced electron transfer; this state is formed within 13–21 ps, and decays on a time scale of ca. 200 ps. In the presence of a competing guest with a large binding constant (cycloundecanone) which displaces each electron-accepting quencher from the cage cavity, the charge-separated state is no longer observed. Further, a combination of mononuclear {Os­(NN)3}2+ model complexes with the same electron-accepting species showed no evidence for formation of charge-separated Os­(III)/guest•– states. These two control experiments indicate that the {Os­(NN)3}2+ chromophores need to be assembled into the cage structure to bind the electron-accepting guests, and for PET to occur. These results help to pave the way for use of photoactive coordination cages as hosts for photoredox catalysis reactions on bound guests.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.8b02860