S. A. Iberoamericana, (b) P. Atkins, Fisicoquímica, Third Edition in Spanish, p.845, 1986.

A. Magistrato, T. Woo, A. Togni, and U. Rothlisberger, Enantioselective Palladium-Catalyzed Hydrosilylation of Styrene:?? Detailed Reaction Mechanism from First-Principles and Hybrid QM/MM Molecular Dynamics Simulations, Organometallics, vol.23, issue.13, p.3218, 2004.
DOI : 10.1021/om049969c

Y. Wang, S. Ou, P. Liu, F. Xue, and S. Tang, Comparison of two different processes to synthesize biodiesel by waste cooking oil, Journal of Molecular Catalysis A: Chemical, vol.252, issue.1-2, pp.107-135, 2006.
DOI : 10.1016/j.molcata.2006.02.047

J. Osborn, F. Jardine, J. Young, G. Wilkinson, J. J. Birch et al., 10 (a) A Advanced Inorganic Chemistry (b) C. Masters, Homogeneous Transition-metal Catalysis-A Gentle Art, Chem. Soc. A J. Am. Chem. Soc.C. Phillips, J. Am. Chem. Z. Anorg. Chem, vol.24, issue.16 6, pp.155-661, 1711.

T. Sabel and . Takahashi, Titanium(IV) Chloride-Triethylaluminum": Encyclopedia of Reagents for Organic Synthesis, Angew. Chem., Int. Ed. Engl. Coord. Chem. Rev, vol.156, issue.1 16, pp.80-95, 1962.

. Bis, II))-?-s-indacenediide 22a: A solution of n-BuLi (3.68 mL, 5.88 mmol) in hexane (1.6 M) is added to a solution of 8b (0.70 g, 2.94 mmol) in THF (25 mL) at -80°C. The reaction mixture is allowed to reach room temperature and stirred for 1.5 hours, followed by stirring at 50°C for another 2 hours. The solution was cooled to -80°C and 17 (1.60 g, 1.47 mmol) in THF (30 mL) was slowly added via syringe. The mixture was allowed to reach room temperature and stirred for 2 hours. The solvents were evaporated under reduced pressure, To the remaining solid, 15 mL of toluene was added and the insoluble lithium chloride is removed by filtration. (Yield: 1.84 g, 88%), p.5

. Anti-isomer-22c, Melting Point (sealed capillary, pp.196-203

J. Manriquez, M. Ward, and W. , References Chapter 3: Synthesis and Spectroscopic Study of Organometallic Complexes 150 1 (a), 100%) [Rh(COD) · ] + = 211 (39%)

F. Cotton, G. Wilkinson, C. Murillo, and M. Bochman, Advanced Inorganic Chemistry, p.661, 1999.

F. G. Bordwell and P. S. Landis, Elimination Reactions. VII. A Comparison of Some Eliminations in Open-chain and Cyclic Systems, Journal of the American Chemical Society, vol.79, issue.7, p.1593, 1957.
DOI : 10.1021/ja01564a020

A. R. Cutler, P. K. Hanna, and J. C. Vites, Carbon monoxide and carbon dioxide fixation: relevant C1 and C2 ligand reactions emphasizing (.eta.5-C5H5)Fe-containing complexes, Chemical Reviews, vol.88, issue.7, p.1363, 1988.
DOI : 10.1021/cr00089a016

. Here, 7 mmHg, forming a mixture of HS2 and DS Products in solution, There were analyzed as a mixture by NMR tools, and further characterized by GC-MS techniques

B. Boury, R. Corriu, D. Peclercq, P. Mutin, J. Planeix et al., The Chemistry of Organic Silicon Compounds, 21. b) S, 1457.

P. Pawluc, B. Marciniec, I. Kownacki, and H. Maciejewski, Synthesis of phenylene???silylene???ethylene polymers via transition metal complex catalyzed hydrosilylation polymerization, Applied Organometallic Chemistry, vol.36, issue.1, p.49, 2005.
DOI : 10.1002/aoc.819

A. Ini, T. Oliver, R. Tilley, and . Bergman, Synthesis, Structure, and Hydrosilylation Catalysis of a Chiral A-Frame Rhodium(I) Dimer with Cis Diphosphite Ligands, Organometallics, vol.20, issue.18, p.3839, 2001.
DOI : 10.1021/om010428m

C. Bonifaci, G. Carta, A. Ceccon, A. Gambaro, and S. Santi, ] with Olefins, Organometallics, vol.15, issue.6, p.1630, 1996.
DOI : 10.1021/om950775u

J. Orsini and W. E. Geiger, Electrochemical Characterization of Equilibria Involving Catalyst Precursors:?? Cyclic Voltammetry of Labile Organorhodium Complexes in Coordinating Solvents, Organometallics, vol.18, issue.10, p.1854, 1999.
DOI : 10.1021/om9900566

M. Martín, E. Sola, O. Torres, P. Plou, and L. Oro, Versatility of Cyclooctadiene Ligands in Iridium Chemistry and Catalysis, Organometallics, vol.22, issue.26, p.5406, 2003.
DOI : 10.1021/om034218g