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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container_issue 4
container_start_page 2386
container_title Inorganic chemistry
container_volume 58
creator 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
description 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.
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P ; Argent, Stephen P ; Weinstein, Julia A ; Ward, Michael D</creator><creatorcontrib>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</creatorcontrib><description>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. 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P</creatorcontrib><creatorcontrib>Argent, Stephen P</creatorcontrib><creatorcontrib>Weinstein, Julia A</creatorcontrib><creatorcontrib>Ward, Michael D</creatorcontrib><title>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</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>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. 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Chem</addtitle><date>2019-02-18</date><risdate>2019</risdate><volume>58</volume><issue>4</issue><spage>2386</spage><epage>2396</epage><pages>2386-2396</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>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. 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