Synthesis and Characterization of New Sandwiched and multi Decker Palladium Organometallic Compounds of alkylated S-Indacene

Authors

  • Pasha K M Mussuvir Department of Chemistry, Vijayanagara Sri Krishnadevaraya University, Jnana Sagara Campus, Ballari, Karnataka-583105, India
  • Mallikarjuna G Patil PG Department of Chemistry, Basaveshwara Science College, Bagalkote Karnataka India.
  • M K Amshumali Assistant Professor, Department of Chemistry/Industrial Chemistry, Vijayanagara Sri Krishnadevaraya university, Jnanasagara campus, Cantonment, Bellary, Karnataka 583105, India

DOI:

https://doi.org/10.48165/

Keywords:

palladium organometallics, s indacene, multidecker, sandwich

Abstract

A synthesis of mono nuclear bis indacene mono  metal compound of type [L-M-L] where (L is 2,6- diethyl-4,8-dimethyl-1,5-dihydro-s-indacene, M=Pd. Pd-bis (ƞ5-2,6-diethyl-4,8-dimethyl-1,5- dihydro-s-indaceneide) [Pd (Ic’H)2], and the  oligomeric form of this compound is successfully  prepared. The prepared compound is of the type  [L-M-L-M-L-M-L] where M= Pd and L =-2,6- diethyl-4,8-dimethyl-1,5-dihydro-s-indaceneide)}]  [Ic’Pd(µ-Ic’) Pd (µ-Ic’)PdIc’] the reaction yields a  almost quantitative yield. The synthesized  compounds were characterized by NMR (1H and 13C), and elemental analysis. The spectroscopic  data reveals the formation Multidecker  compound. This oligomer is further subjected to  catalytic property study 

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References

Metal-catalyzed Cross-coupling Reactions; Diederich, F.; Stang, P. J. Eds.; Wiley-VCH: Weinhein, Germany, 1998.

Farina, V.; Krishnamurthy, V.; Scott, W. J. The Stille Reaction: Wiley, New York, NY, 1998. 3. Tsuji, J. Perspectives in Organopalladium Chemistry for the 21st Century: Elsevier, Lausanne, Switzerland, 1999.

Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis: Wiley, Chichester, UK, 1995.

Hegedus, L. S. Transition Metals in the Synthesis of Complex Organic Molecules 2nd Ed.,: University Science Books, Mill Valley, USA, 1999.

Malleron, J.-L.; Fiaud, J.-C.; Legros, J.-Y. Handbook of Palladium-catalyzed Organic Reactions: Academic Press, San Diego, USA, 1997

M. J. H. Russell Johnson Matthey, Materials Technology Division, Royston. An Advantageous Use of Palladium Compounds in Organic Synthesis The Formation of Carbon-Carbon Bonds, Platinum Metals Rev., 1989, 33, (4), 186

For an early review, see: Hegedus, L. S. Angew. Chem., Int. Ed. Engl. 1988, 27, 1113–126. 9. For a recent review, see: Fujiwara, Y.; Jia, C. in Handbook of Organopalladium Chemistry for Organic Synthesis, Negishi, E.-i. Ed.; John Wiley and Sons: Hoboken, 2002, vol. 2, pp. 2859–62. 10. Åkermark, B.; Eberson, L.; Jonsson, E.; Pettersson, E. J. Org. Chem. 1975, 40, 1365–7. 11. Knölker, H.-J.; Fröhner, W. J. Chem. Soc., Perkin Trans. 1 1998, 173–6.

Knölker, H.-J.; O’Sullivan, N. Tetrahedron 1994, 50, 10893–908.

Suzuki, A. in Modern Arene Chemistry, Astruc, D., Ed.; Wiley-VCH: Weinheim, 2002, pp. 53–106.

Miyaura, N. in Metal-Catalyzed Cross-Coupling Reactions, deMeijere, A.; Diederich, F., Eds.; 2nd Ed., Wiley-VCH: Weinheim, 2004, pp. 41–123.

Kotha, S.; Lahiri, K.; Kashinath, D. Tetrahedron 2002, 58, 9633–95.

Negishi, E.-i.; Baba, S. J. Chem. Soc., Chem. Commun. 1976, 596–7.

Negishi, E.-i. Acc. Chem. Res. 1982, 15, 340–8.

Negishi, E.-i. in Handbook of Organopalladium Chemistry for Organic Synthesis, Negishi, E.-i. Ed.; John Wiley and Sons: Hoboken, 2002, vol. 1, pp. 229–47.

J. P. Wolfe and J. Jack Li, Tetrahedron Org. Chem. Ser., 2007, 26, 1–35.

C. Creutz, H. Taube, J. Am. Chem. Soc., 1969, 91, 3988.

C. Creutz, H. Taube, J. Am. Chem. Soc., 1973, 95, 1086

B. Oelckers, I. Chavez, J.M. Manriquez, E. Román, Organometallics 12 (1993) 3396 23. M.R. Dahrouch, P. Jara, L. Mendez, Y. Portilla, D. Abril, G. Alfonso, I. Chavez, J.M. Manriquez, M. Rivière-Baudet, P. Rivière, A. Castel, J. Rouzaud, H. Gornitzka, Organometallics 20 (2001) 5591 24. F. Lissel, T. Fox, O. Blacque, W. Polit, R.F. Winter, K. Venkatesan, H. Berke, J. Am. Chem. Soc. 135 (2013) 4051.

D.M. D’Alessandro, F.R. Keene, Chem. Rev. 106 (2006) 2270

Purification of laboratory chemicals book authored by Amerigo W. L., Perrin D 27. M.R. Dahrouch, P. Jara, L. Mendez, Y. Portilla, D. Abril, G. Alfonso, I. Chavez, J.M.Manriquez, M. Riviere-Baudet, P. Riviere, A. Castel, J. Rouzaud, H. Gornitzka, Organometallics 20 (2001) 5591. 28. O. Hayden, C.K. Payne, Angew. Chem., Int. Ed. 44 (2005) 1395.

X. Duan, Y. Huang, Y. Cui, J. Wang, C.M. Lieber, Nature 409 (2001) 66.

J. Wild, J. Org. Chem., 1982, 232, 233.

H. Amouri, J. Vaissermann, M. N. Rager, Y. Besace, Inorg. Chem., 1999, 38, 1211. 32. C. Morales-Verdejo, I. Martínez-Díaz, C. Adams, J. F. Araneda, L. Oehninger, D. Mac-Leod Carey, A. Muñoz-Castro, R. Arratia-Pérez, I. Chávez and J. M. Manríquez, Polyhedron, , DOI:10.1016/j.poly.2013.11.023.

Published

2019-05-05

How to Cite

Synthesis and Characterization of New Sandwiched and multi Decker Palladium Organometallic Compounds of alkylated S-Indacene . (2019). Bulletin of Pure and Applied Sciences-Chemistry , 38(1), 89–94. https://doi.org/10.48165/