Structure-activity relationship between some novel silica supported palladium catalysts: A study of the Suzuki reaction

Journal of Molecular Catalysis A: Chemical

Volumn 215, Issue 1-2, 2004, Pages 107-111

  Paul, Satya ^a   Clark, James H ^b  

^a UNIVERSITY OF JAMMU   (India)

^b UNIVERSITY OF YORK   (United Kingdom)

Author keywords

Heterogeneous catalysis; Silica supported palladium catalysts; Structure activity relationship; Suzuki coupling; X ray photoelectron spectroscopy

Indexed keywords

BINDING ENERGY; CHELATION; PALLADIUM; POTASSIUM COMPOUNDS; RATE CONSTANTS; SILICON; SURFACE ACTIVE AGENTS; SYNTHESIS (CHEMICAL); X RAY PHOTOELECTRON SPECTROSCOPY; XYLENE;

BROMOBENZENE; PALLADIUM CATALYSTS; STRUCTURE-ACTIVITY RELATIONSHIP; SUZUKI REACTION;

CATALYSIS;

2 ACETYLFURAN; 2 ACETYLPYRIDINE; 2 AMINOACETOPHENONE; 2 FURANCARBOXALDEHYDE; 2 HYDROXYACETOPHENONE; 2 PYRROLECARBOXALDEHYDE; 2 THIOPHENECARBOXALDEHYDE; 3 AMINOPROPYL(TRIMETHOXY)SILANE; 3 AMINOPROPYLSILICA; ACETOPHENONE DERIVATIVE; ALDEHYDE DERIVATIVE; BENZENEBORONIC ACID; BROMOBENZENE; CHELATING AGENT; FURAN DERIVATIVE; LIGAND; ORTHO XYLENE; PALLADIUM ACETATE; PALLADIUM COMPLEX; POTASSIUM CARBONATE; PYRIDINE DERIVATIVE; PYRIDINECARBOXALDEHYDE; SCHIFF BASE; SILANE DERIVATIVE; SILICON DIOXIDE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; ATOM; CATALYSIS; CATALYST; CHEMICAL ANALYSIS; ENERGY; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION; SUZUKI REACTION; X RAY PHOTOELECTRON SPECTROSCOPY;

EID: 1942436178     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2003.12.034     Document Type: Article

References (18)

1. J.N. Armor (Ed.), Environmental Catalysis, ACS Symposium Series, 1994, p. 552.
2. G. Ertl, H. Knozinger, J. Weitkamp, Environmental Catalysis, Wiley/VCH, Weiheim, Germany, 1999.
3. P.T. Anastas, J.C. Warner, Green Chemistry: Theory and Practice, Oxford University Press, Oxford, 1998.
4. P.T. Anastas, L.G. Heine, T.C. Williamson (Eds.), Green Chemical Synthesis and Processes: Recent Advances in Chemical Processing, The American Chemical Society, Washington, DC, 2001.
5. Tundo P., Anastas P., Black D.S., Breen J., Collins T., Memoli S., Miyamoto J., Ployakoff M., Tumas W. Pure Appl. Chem. 72:2000;1207.
6. de Miguel Y.R. J. Chem. Soc. Perkin Trans. 1:2000;4213-4221.
7. Corain B., Kralik M. J. Mol. Catal. A Chem. 173:2001;99-115.
8. McNamara C.A., Dixon M.J., Bradley M. Chem. Rev. 102:2002;3275-3300.
9. Leadbeater N.E., Marco M. Chem. Rev. 102:2002;3217-3274.
10. Clark J.H., Macquarrie D.J., Mubofu E.B. Green Chem. 2:2000;53-55.
11. Clark J.H., Macquarrie D.J., Mubofu E.B. Green Chem. 3:2001;23-25.
12. M. Julia, M. Dutheil, Bull. Soc. Chem. Chim. Fr. (1973) 2791.
13. Yamada Y.M.A., Takeda K., Takahashi H., Ikegami S. Tetrahedron Lett. 44:2003;2379-2382.
14. Kohler K., Wagner M., Djakovitch L. Catal. Today. 66:2001;105-114.
15. C. Baleizao, A. Corma, H. Garcia, A. Leyva, Chem. Commun. (2003) 606-607.
16. Okubo K., Shirai M., Yokoyama C. Tetrahedron Lett. 43:2002;7115-7118.
17. Lagasi M., Moggi P. J. Mol. Cat. A Chem. 182-183:2002;61-72.
18. Paul S., Clark J.H. Green Chem. 5:2003;635-638.