Erratum: Novel improved ruthenium catalysts for the generation of hydrogen from alcohols (Chemical Communications (2007) DOI: 10.1039/b613785g);Novel improved ruthenium catalysts for the generation of hydrogen from alcohols

Chemical Communications

Volumn , Issue 5, 2007, Pages 522-524

  Junge, Henrik ^a   Loges, Björn ^a   Beller, Matthias ^a  

^a UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2 PROPANOL; ALCOHOL; AMINE; CHLORIDE; HYDROGEN; LIGAND; PARA CYMENE; RUTHENIUM;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; DEHYDROGENATION; TEMPERATURE;

EID: 33846526624     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b700283c     Document Type: Erratum

References (46)

1. M. Eingartner, G. Eisenbeiß and M. Fuchs, Wasserstoff part X, Informationsschriften der VDI-Gesellschaft Energietechnik: Reihe Regenerative Energien, VDI - GET, Düsseldorf, 1996
2. C.-J. Winter and J. Nitsch, Wasserstoff als Energieträger, Springer Verlag, Berlin, 1989
3. M. R. Hoffmann S. T. Martin W. Choi D. M. Bahnemann Chem. Rev. 1995 95 69
4. O. Legrini E. Oliveros A. M. Braun Chem. Rev. 1993 93 671
5. W. Gerhartz, C. Mayer, P. Monkhouse and R. Pfefferkorn, Ullmanns Encyclopädie der technischen Chemie, Band 24, 4. Auflage, Verlag Chemie, Weinheim, 1983, pp 275-289
6. Y. Ando M. Yamashita Y. Saito Bull. Chem. Soc. Jpn. 2003 76 2045
7. J. Llorca P. Ramirez de la Piscina J.-A. Dalmon N. Homs Chem. Mater. 2004 16 3573
8. D. K. Liguras K. Goundani X. E. Verykios Int. J. Hydrogen Energy 2004 29 419
9. F. Aupretre C. Descorme D. Duprez Fr. Annal. Chim. 2001 26 93
10. R. R. Davda J. A. Dumesic Angew. Chem. 2004 116 1575
11. R. R. Davda J. A. Dumesic Chem. Commun. 2004 36
12. R. D. Cortright R. R. Davda J. A. Dumesic Nature 2002 418 964
13. R. R. Davda J. A. Dumesic Angew. Chem. 2003 115 4202 Angew. Chem., Int. Ed 2003 42 3971
14. J. S. M. Samec J.-E. Bäckvall P. G. Andersson P. Brandt Chem. Soc. Rev. 2006 35 237
15. S. Gladiali E. Alberico Chem. Soc. Rev. 2006 35 226
16. S. Gladiali and E. Alberico, in Transition Metals in Organic Synthesis Vol. 2, ed., M. Beller, C. Bolm, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2nd edn, 2004, pp 145-166
17. A. Dobson St. D. Robinson Inorg. Chem. 1977 16 137
18. W. K. Rybak J. J. Ziolkowski J. Mol. Catal. 1981 11 365
19. C. W. Jung P. E. Garrou Organometallics 1982 1 658
20. G. B. W. L. Ligthart R. H. Meijer M. P. J. Donners J. Meuldijk J. A. J. M. Vekemans L. A. Hulshof Tetrahedron Lett. 2003 44 1507
21. D. Morton D. J. Cole-Hamilton J. Chem. Soc., Chem. Commun. 1988 1154
22. D. Morton D. J. Cole-Hamilton D. Utuk M. Paneque-Sosa M. Lopez-Poveda J. Chem. Soc., Dalton Trans. 1989 489
23. L.-C. Yang T. Ishida T. Yamakawa S. Shinoda J. Mol. Catal. 1996 108 87
24. T. Fujii Y. Saito J. Mol. Catal. 1991 67 185
25. S. Shinoda H. Itagaki Y. Saito J. Chem. Soc., Chem. Commun. 1985 860
26. R. Jackstell S. Harkal H. Jiao A. Spannenberg C. Borgmann D. Röttger F. Nierlich M. Elliot S. Niven K. Cavell O. Navarro M. S. Viciu S. P. Nolan M. Beller Chem.-Eur. J. 2004 10 3891
27. A. Moballigh A. Seayad R. Jackstell M. Beller J. Am. Chem. Soc. 2003 125 10311
28. A. Seayad M. Ahmed H. Klein R. Jackstell T. Gross M. Beller Science 2002 297 1676
29. K. Selvakumar A. Zapf M. Beller Org. Lett. 2002 4 3031
30. R. Jackstell H. Klein M. Beller K.-D. Wiese D. Röttger Eur. J. Org. Chem. 2001 3871
31. H. Junge M. Beller Tetrahedron Lett. 2005 46 1031
32. J. Zhang G. Leitus Y. Ben-David D. Milstein J. Am. Chem. Soc. 2005 127 10840
33. J. Zhang M. Gandelmann L. Shimon H. Rozenberg D. Milstein Organometallics 2004 24 4026
34. G. R. A. Adair J. M. J. Williams Tetrahedron Lett. 2005 46 8233
35. J. H. Choi N. Kim Y. J. Shin J. H. Park J. Park Tetrahedron Lett. 2004 45 4607
36. J. van Buijtenen J. Meuldijk J. A. J. M. Vekemans L. A. Hulshof H. Kooijman A. L. Spek Organometallics 2006 25 873
37. J. Zhao J. F. Hartwig Organometallics 2005 24 2441
38. All experiments were carried out under an inert gas atmosphere (argon) with exclusion of air. For the standard reaction procedure sodium is dissolved in 4.0/8.0/38.0 mL of isopropanol at 90°C in a double walled thermostated reaction vessel. This vessel is vigorously purged with argon to remove any hydrogen before starting the catalytic reaction. Hexadecane, 0.5/1.0/4.0 mL, has been added as internal standard. The solution containing the catalyst and the ligand in 1.0/2.0 mL isopropanol is prepared in a Schlenk tube and added to the reaction vessel at 90°C via septa and a small teflon tube after refluxing became stationary. Starting with the addition of the catalyst the progress of the reaction is followed by several analytical methods. The amount of generated hydrogen is measured by gas burette. In addition a hydrogen sensor of the Fa. Hach Ultra Analytics GmbH is used for analysis of hydrogen and a GC for analyzing gases is applied (gas chromatograph HP 5890, permanent gases: Carboxen 1000, TCD, external calibration; alkanols, aldehydes/ketones: HP Plot Q, 30 m, FID). Aldol condensation products and hydrogenation of the aldol condensation products are analyzed by gas chromatography (HP 1, 50 m, FID, internal standard). Typically, the reproducibility of the volumetric determined hydrogen is between 5-15%
39. C. Carlini M. D. Girolamo A. Macinai M. Marchionna M. Noviello A. M. Raspolli Galletti G. Sbrana J. Mol. Catal. 2003 204 721
40. C. Carlini A. Macinai M. Marchionna M. Noviello A. M. Raspolli Galletti G. Sbrana J. Mol. Catal. 2003 206 409
41. -1)
42. W. Barratta E. Herdtweck K. Siega M. Toniutti P. Rigo Organometallics 2005 24 1660
43. T. Riermeier P. Gross A. Monsees M. Hoff H. Trauthwein Tetrahedron Lett. 2005 46 3403
44. M. Gomez S. Jansat G. Muller G. Aullon M. A. Maestro Eur. J. Inorg. Chem. 2005 4341
45. A. S. Y. Yim M. Wills Tetrahedron 2005 61 7994
46. G. Csjernyik K. Bogar J.-E. Bäckvall Tetrahedron Lett. 2004 45 6799