Experiments with the titanium dioxide-ruthenium tris -bipyridine-nickel cyclam system for the photocatalytic reduction of CO2

Green Processing and Synthesis

Volumn 2, Issue 4, 2013, Pages 335-343

  Montanaro, Sara ^a   Herrero, Christian ^b,c   Merli, Daniele ^a   Fagnoni, Maurizio ^a   Poggi, Antonio ^a   Protti, Stefano ^a   Sheth, Sujitraj ^b   Albini, Angelo ^a  

^a UNIVERSITY OF PAVIA   (Italy)

^b SERVICE DE CHIMIE BIOORGANIQUE ET DE MARQUAGE   (France)

^c UNIVERSITÉ PARIS SUD   (France)

Author keywords

CO2 reduction; Photocatalysis; Ruthenium (II) tris bipyridine; Titanium dioxide

Indexed keywords

CARBON DIOXIDE; RUTHENIUM COMPOUNDS; TITANIUM DIOXIDE;

BIPYRIDINES; CO 2 REDUCTION; COVALENT BINDING; FUNCTIONALIZED; PHOTOCATALYTIC REDUCTION; RUTHENIUM (II) TRIS -BIPYRIDINE; RUTHENIUM TRIS(BIPYRIDINE); SENSITISER; TITANIA; ]+ CATALYST;

NICKEL;

EID: 84944311823     PISSN: 21919542     EISSN: 21919550     Source Type: Journal    
DOI: 10.1515/gps-2013-0040     Document Type: Article

References (45)

1. Yang H, Xu Z, Fan M, Gupta R, Slimane RB, Bland AE, Wright I. J. Environ. Sci. 2008, 20, 14-27.
2. Yu CH, Huang CH, Tan CS. Aerosol Air Qual. Res. 2012, 12, 745-769.
3. Liu J, Thallapally PK, McGrail BP, Brown DR, Liu J. Chem. Soc. Rev. 2012, 41, 2308-2322.
4. Sakakura T, Choi JC, Yasuda H. Chem. Rev. 2007, 107, 2365-2387.
5. Grills DC, Fujita E. J. Phys. Chem. Lett. 2010, 1, 2709-2718.
6. Fujita E. Coord. Chem. Rev. 1999, 185 - 186, 373-384.
7. Habisreutinger SN, Schmidt-Mende L, Stolarczyk JK. Angew. Chem. Int. Ed. 2013, 52, 7372-7408.
8. Beley M, Collin JP, Ruppert R, Sauvage JP. J. Am. Chem. Soc. 1986, 108, 7461-7467.
9. Saravanakumar D, Song J, Jung N, Jirimali H, Shin W. ChemSusChem 2012, 5, 634-636.
10. Froehlich JD, Kubiak CP. Inorg. Chem. 2012, 51, 3932-3934.
11. Hawecker J, Lehn JM, Ziessel R. J. Chem. Soc. Chem. Commun. 1983, 536-538.
12. Craig CA, Spreer LO, Otvos JW, Calvin M. J. Phys. Chem . 1990, 94, 7957-7960.
13. Grant JL, Goswami K, Spreer LO, Otvos JW, Calvin M. J. Chem. Soc. Dalton Trans. 1987, 2105-2109.
14. Mochizuki K, Manaka S, Takeda I, Kondo T. Inorg. Chem. 1996, 35, 5132-5136.
15. Reithmeier R, Bruckmeier C, Rieger B. Catalysts 2012, 2, 544-571.
16. Ogata T, Yamamoto Y, Wada Y, Murakoshi K, Kusaba M, Nakashima N, Ishida A, Takamuku S, Yanagida S. J. Phys. Chem . 1995, 99, 11916-11922.
17. Creutz C, Chou M, Netzel TN, Okumura M, Sutin N. J. Am. Chem. Soc. 1980, 102, 1309-1319.
18. Gust D, Moore TA, Moore AL. Acc. Chem. Res. 2009, 42, 1890-1898.
19. Herrero C, Lassalle-Kaiser D, Leibl W, Rutherford AW, Aukauloo W. Coord. Chem. Rev. 2008, 252, 456-468.
20. Ishai MA, Yoon TP. Eur. J. Org. Chem. 2012, 3359-3372.
21. Ravelli D, Fagnoni M, Albini A. Chem. Soc. Rev. 2013, 42, 97-113.
22. Otero MD, Batanero B, Barba F. Tetrahedron Lett. 2006, 47, 2171-2173.
23. Kimura E, Bu X, Shionoya M, Wada S, Maruyama S. Inorg. Chem. 1992, 31, 4542-4546.
24. Woolerton TW, Sheard S, Reisner E, Pierce E, Ragsdale SW, Armstrong FA. J. Am. Chem. Soc. 2010, 132, 2132-2133.
25. Koci K, Obalova L, Lacny Z. Chem. Papers 2008, 62, 1-9.
26. Indrakanti VP, Kubickib JD, Schobert HH. Energy Environ. Sci. 2009, 2, 745-758.
27. Sato S, Morikawa T, Saeki S, Kajino T, Motohiro T. Angew. Chem. Int. Ed. 2010, 49, 5101-5105.
28. Nazeeruddin MK, Kay A, Rodicio L, Humpbry-Baker R, Miiller E, Liska P, Vlachopoulos N, Gratzel MM. J. Am. Chem. Soc . 1993, 115, 6382-6390.
29. McNamara WR, Snoeberger RC III, Li G, Richter C, Allen L, Milot RL, Schmuttenmaer CA, Crabtree RH, Brudvig GW, Batista WS. Energy Environ. Sci. 2009, 2, 1173-1175.
30. Trammell SA, Wimbish JC, Odobel F, Gallagher LZ, Narula PM, Meyer TJ. J. Am. Chem. Soc. 1998, 120, 13248-13249.
31. Hanson K, Brennaman KMK, Luo H, Glasson CRK, Concepcion JJ, Song W, Meyer TJ. ACS Appl. Mater. Interfaces 2012, 4, 1462-1469.
32. Beer PD, Szemes F, Balzani V, Sala CM, Drew MGB, Dent SW, Maestri M. J. Am. Chem. Soc. 1997, 119, 11864-11875.
33. Koola JD, Kochi JK. Inorg. Chem. 1987, 26, 908-916.
34. Simpson P, Vinciguerra A, Quagliano J. Inorg. Chem. 1963, 2, 282-286.
35. Anderson S, Constable EC, Seddon KR, Turp JE, Baggott JE, Pilling MJ. J. Chem. Soc., Dalton Trans. 1985, 2247-2261.
36. Staats H, Eggers F, Ha s O, Fahrenkrug F, Matthey J, Lüning U, Lutzen A. Eur. J. Org. Chem. 2009, 4777-4792.
37. Wenkert D, Woodward R. J. Org. Chem. 1983, 48, 283-289.
38. Maerker G, Case FH. J. Am. Chem. Soc. 1958, 80, 2745-2748.
39. Penicaud V, Odobel F, Bujoli B. Tetrahedron Lett. 1998, 39, 3689-3692.
40. Gillaizeau-Gauthier I, Odobel F, Alebbi M, Argazzi, R, Costa, E, Bignozzi CA, Qu P, Meyer GJ. Inorg. Chem. 2001, 40, 6073-6079.
41. Ardo S, Sun Y, Staniszewski A, Castellano FN, Meyer GJ. J. Am. Chem. Soc. , 2010, 132, 6696-6709.
42. Patterson BT, Keene FR. Aus. J. Chem. 1998, 51, 999-1002.
43. Rehm D, Weller A. Isr. J. Chem. 1970, 8, 259-271
44. Creutz C, Sutin N. J. Am. Chem. Soc. 1976, 98, 6384-6385.
45. Brennaman MK, Patrocinio AOT, Song W, Jurss JW, Concepcion JJ, Hoertz PJ, Traub MC, Murakami Iha NY, Meyer TJ. ChemSusChem 2011, 4, 216-227.