Prof. Dr. Pedro Maximo Emilio Mancini
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Prof. Dr. Pedro Maximo Emilio Mancini

Professor
Universidad Nacional del Litoral, Argentina

Highest Degree
PostDoc. in Chemistry from University of California, Los Angeles, USA

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Area of Interest:

Chemistry
100%
Organic Chemistry
62%
Analytical Chemistry
90%
Chemical Reaction
75%
Chemical Engineering
55%

Research Publications in Numbers

Books
0
Chapters
0
Articles
0
Abstracts
0

Selected Publications

  1. Guntero, V.A., C.A. Ferretti, P.M.E. Mancini and M.N. Kneeteman, 2018. Encapsulation of compounds biphenyls into SBA-15: Synthesis of composites for application. Global J. Eng. Sci. Res., 5: 32-39.
  2. Guntero, V., C. Ferretti, P.M.E. Mancini and M.N. Kneeteman, 2018. Teaching of chemistry applied: Development of a laboratory-scale fire started. World J. Chem. Educ., 6: 87-90.
  3. Mancini, P.M.E., M.N. Kneeteman, M. Cainelli and C.M. Ormachea, 2017. Cycloaddition reactions assisted by microwave irradiation: Protic ionic liquids vs solvent-free conditions. Curr. Microwave Chem., 4: 219-228.
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  4. Mancini, P.M.E., M. Cinelli, C.M. Ormachea and M.N. Kneeteman, 2017. Se of Furan Derivatives Acting as Electrophilic Dienophiles: An Experimental and Theoretical Analysis of Polar Cycloaddition Reactions. In: Advances in Chemistry Research, Taylor, C. (Ed.). Vol. 37, NOVA Publisher, USA., pp: 177-206.
  5. Mancini, P.M., M.N. Kneeteman, M. Cainelli, C.M. Ormachea and L.R. Domingo, 2017. Nitropyrroles, Diels-Alder reactions assisted by microwave irradiation and solvent effect. An experimental and theoretical study. J. Molecular Struct., 1147: 155-160.
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  6. Guntero, V.A., P.M. Mancini and M.N. Kneeteman, 2017. Introducing organic chemistry students to the extraction of natural products found in vegetal species. World, 5: 142-147.
  7. Guntero, V., M.N. Kneeteman and P.M.E. Mancini, 2017. Preparation of gel alcohol flavored with essential oils. An employ of laboratory techniques in the organic chemistry study. World J. Chem. Educ., 5: 86-90.
  8. Cainelli, M., C. Ormachea, M. Kneeteman and P. Mancini, 2016. A theoretical study of the Diels-Alder reaction between 3-nitrofuran and different dienes developed in ionic liquids. Int. J. Pure Applied Chem., 12: 1-10.
  9. Ormachea, C.M., P.M. Mancini, M.N. Kneeteman and L.R. Domingo, 2015. Understanding the participation of 3-nitropyridine in polar Diels-alder reactions. A DFT study. Comput. Theoretical Chem., 1072: 37-42.
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  10. Kneeteman, M.N., A.F.L. Baena, C.D. Rosa and P.M. Mancini, 2015. Polar diels-alder reactions using heterocycles as electrophiles. Influence of microwave irradiation. Int. Res. J. Pure Applied Chem., 8: 229-235.
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  11. Della Rosa, C.D., P.M. Mancini, M.N. Kneeteman, A.F.L. Baena, M.A. Suligoy and L.R. Domingo, 2015. Polar diels-alder reactions using electrophilic nitrobenzothiophenes. A combined experimental and DFT study. J. Mol. Struct., 1079: 47-53.
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  12. Costero, A.M., S. Gil, M. Parra, P.M. Mancini, M.N. Kneeteman and M.I. Quindt, 2015. 5, 5'-Bis-vanillin derivatives as discriminating sensors for trivalent cations. Tetrahedron Lett., 56: 3988-3991.
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  13. Ormachea, C., M.N. Kneeteman and P. Mancini, 2014. Pseudo-pericyclic reactions: Aromatic compound derivatives as electrophiles in polar diels-alder reactions. An experimental and theoretical study. Rev. Res. Trends, 17: 73-91.
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  14. Kneeteman, M.N., C.D. Della Rosa, C.M. Ormachea, P. Gimenez, A.F. Lopez Baena and P.M.E. Mancini, 2014. Synthesis of phenanthrenol derivatives through polar diels-alder reactions employing nitronaphthalenes and (E)-1-(Trimethylsilyloxy)-1, 3-butadiene. Theoretical calculations. Lett. Organic Chem., 11: 333-337.
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  15. Adam, C.G., M. Bravo, P.M. Mancini and G.G. Fortunato, 2014. Solvatochromic dipolarity micro‐sensor behaviour in binary solvent systems of the (water+ ionic liquid) type: Application of preferential solvation model and linear solvation energy relationships. J. Phys. Organic Chem., 27: 841-849.
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  16. Adam, C., M.V. Bravo and P.M. Mancini, 2014. Molecular solvent effect on the acidity constant of protic ionic liquids. Tetrahedron Lett., 55: 148-150.
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  17. Mancini, P.M.E., M.N. Kneeteman, C. Della Rosa, C. Ormachea and L.R. Domingo, 2013. Protic and Nonprotic Ionic Liquids in Polar Diels-Alder Reactions using Properly Substituted Heterocycles as Dienophiles. A DFT Study. In: Ionic Liquids-New Aspects for the Future, Kadakawa, J. (Ed.). INTECH Publisher, USA., pp: 391-413.
  18. Mancini, P.M., C.D. Della Rosa, C.M. Ormachea, M.N. Kneeteman and L.R. Domingo, 2013. Experimental and theoretical studies on polar Diels-Alder reactions of 1-nitronaphathalene developed in ionic liquids. RSC Adv., 3: 13825-13834.
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  19. Rosa, C.D.D., C.M. Ormachea, A.S. Sonzogni, M.N. Kneeteman, L.R. Domingo and P.M.E. Mancini, 2012. Polar diels-alder reactions developed in a protic ionic liquid: 3-Nitroindole as dienophile. Theoretical studies using DFT methods. Lett. Organic Chem., 9: 691-695.
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  20. Ormachea, C.M., A.F.L. Baena, C. Della Rosa, M.N. Kneeteman and P.M. Mancini, 2012. N-tosyl-nitropyrroles as dienophiles in polar cycloaddition reactions developed in protic ionic liquids. J. Chem. Chem. Eng., 6: 661-667.
  21. Mancini, P.M.E., G. Fortunato, M.V. Bravo and C. Adam, 2012. Ionic Liquids: Binary Solvents Mixtures with selected Molecular Solvents: Characterization of its Molecular-Microscopic Properties. In: Green Solvents Properties and Applications in Chemistry, Mohammad, A. and M.P. Inamuddin (Eds.). Springer, UK., pp: 335-362.
  22. Mancini, P.M., C.M. Ormachea, C.D. Della Rosa, M.N. Kneeteman, A.G. Suarez and L.R. Domingo, 2012. Ionic liquids and microwave irradiation as synergistic combination for polar Diels-alder reactions using properly substituted heterocycles as dienophiles. A DFT study related. Tetrahedron Lett., 53: 6508-6511.
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  23. Bravo, V., S. Gil, A.M. Costero, M.N. Kneeteman and U. Llaosa et al., 2012. A new phenanthrene-based bis-oxime chemosensor for Fe (III) and Cr (III) discrimination. Tetrahedron, 68: 4882-4887.
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  24. Brasca, R., M.N. Kneeteman, P.M. Mancini and W.M. Fabian, 2012. Diels-alder reactions for the rational design of benzo [b] thiophenes: DFT-based guidelines for synthetic chemists. J. Mol. Struct., 1010: 158-168.
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  25. Mancini, P.M.E., M.N. Kneeteman, C. Della Rosa, M.V. Bravo and C. Adam, 2011. Ionic Liquids in Polar Diels-Alder Reactions using Carbocicles and Hetrocycles as Dienophiles. In: Ionic Liquids/Classes and Properties, Handy, S. (Ed.). INTECH Publisher, USA., pp: 311-344.
  26. Della Rosa, C., J.P. Sanchez, M.N. Kneeteman and P.M.E. Mancini, 2011. 2-Nitroben‐zofuran and 3-Nitrobenzofurans as dienophiles in polar Diels-Alder reactions. A simple dibenzofurans synthesis. theoretical studies using DFT methods. Tetrahedron Lett., 52: 2316-2319.
  27. Della Rosa, C., C. Ormachea, M.N. Kneeteman, C. Adam and P.M. Mancini, 2011. Diels-Alder reactions of N-tosylpirroles developed in protic ionic liquids. Theoretical studies using DFT methods. Tetrahedron Lett., 52: 6754-6757.
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  28. Brasca, R., M.N. Kneeteman, P.M. Mancini and W.M. Fabian, 2011. Comprehensive DFT study on site‐, regio‐ and stereoselectivity of diels-alder reactions leading to 5‐hydroxybenzofurans. Eur. J. Organic Chem., 2011: 721-729.
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  29. Brasca, R., C. Della Rosa, M. Kneeteman and P.M.E. Mancini, 2011. Five-membered aromatic heterocycles in diels-alder cycloadditio reactions: Theoretical studies as a complement of the experimental researches. Lett. Organic Chem., 8: 82-87.
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  30. Fortunato, G.G., P.M. Mancini, M.V. Bravo and C.G. Adam, 2010. New solvents designed on the basis of the molecular-microscopic properties of binary mixtures of the type (protic molecular solvent+ 1-butyl-3-methylimidazolium-based ionic liquid). J. Phys. Chem. B, 114: 11804-11819.
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  31. Della Rosa, C.D., J.P. Sanchez, M.N. Kneeteman and P.M.E. Mancini, 2010. 2-Nitrobenzofuran as dienophile in polar diels-alder reaction: A simple dibenzofurans synthesis. J. Chem. Chem. Eng., 4: 54-59.
  32. Costero, A.M., M. Parra, S. Gil, R. Gotor and P.M. Mancini et al., 2010. Chromo‐fluorogenic detection of nerve‐agent mimics using triggered cyclization reactions in push-pull dyes. Chem. Asian J., 5: 1573-1585.
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  33. Perez, A.D.C. and P.M. Mancini, 2009. Grouping of hydrogen‐bond ability of pure solvents and their binary mixtures based on the similarity of their microscopic properties. Part 2. J. Phys. Organic Chem., 22: 197-202.
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  34. Brasca, R., M.N. Kneeteman, P.M. Mancini and W.M. Fabian, 2009. Theoretical explanation of the regioselectivity of polar cycloaddition reactions between furan derivatives and Danishefsky's diene. J. Mol. Structure: THEOCHEM, 911: 124-131.
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  35. Adam, C.G., G.G. Fortunato and P.M. Mancini, 2009. Nucleophilic and acid catalyst behavior of a protic ionic liquid in a molecular reaction media. Part 1. J. Phys. Organic Chem., 22: 460-465.
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  36. Mancini, P.M., G.G. Fortunato, C.G. Adam and L.R. Vottero, 2008. Solvent effects on chemical processes: new solvents designed on the basis of the molecular-microscopic properties of (molecular solvent+ 1, 3‐dialkylimidazolium) binary mixtures. J. Phys. Organic Chem., 21: 87-95.
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  37. Domingo, L.R., M.J. Aurell, M. Kneeteman and P.M.E. Mancini, 2008. Toward an understanding of the participation of nitronaphtalenes in polar Diels-Alder reactions. J. Mol. Struct.: THEOCHEM, 853: 68-76.
  38. Costero, A.M., S. Gil, M. Parra, P.M. Mancini, R. Martinez-Manez, F. Sancenon and S. Royo, 2008. Chromogenic detection of nerve agent mimics. Chem. Commun., 2008: 6002-6004.
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  39. Paredes, E., R. Brasca, M. Kneeteman and P.M. Mancini, 2007. A novel application of the Diels-Alder reaction: Nitronaphthalenes as normal electron demand dienophiles. Tetrahedron, 63: 3790-3799.
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  40. Mancini, P.M., C.G. Adam, G.G. Fortunato and L.R. Votteroa, 2007. A comparison of nonspecific solvent scales. Degree of agreement of microscopic polarity values obtained by different measurement methods. Arkivoc, 16: 266-280.
  41. Della Rosa, C., M. Kneeteman and P. Mancini, 2007. Comparison of the reactivity between 2-and 3-nitropyrroles in cycloaddition reactions. A simple indole synthesis. Tetrahedron Lett., 48: 1435-1438.
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  42. Della Rosa, C., M. Kneeteman and P. Mancini, 2007. Behaviour of selenophenes substituted with electron-withdrawing groups in polar Diels-Alder reactions. Tetrahedron Lett., 48: 7075-7078.
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  43. Mancini, P.M., G. Fortunato, C. Adam, L.R. Vottero and A.J. Terenzani, 2002. Specific and non‐specific solvent effects on aromatic nucleophilic substitution. Kinetics of the reaction of 1‐fluoro‐2, 6‐dinitrobenzene and homopiperidine in binary solvent mixtures. J. Phys. Organic Chem., 15: 258-269.
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  44. Biolatto, B., M. Kneeteman, E. Paredes and P.M. Mancini, 2001. Reactions of 1-tosyl-3-substituted indoles with conjugated dienes under thermal and/or high-pressure conditions. J. Organic Chem., 66: 3906-3912.
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  45. Mancini, P.M., A. Terenzani, C. Adam, A.D.C. Perez and L.R. Vottero, 1999. Characterization of solvent mixtures: Preferential solvation of chemical probes in binary solvent mixtures of polar hydrogen‐bond acceptor solvents with polychlorinated co‐solvents. J. Phys. Organic Chem., 12: 713-724.
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  46. Mancini, P.M.E., A. Terenzani, M.G. Gasparri and L.R. Vottero, 1995. Determination of the empirical polarity parameter ET (30) for binary solvent mixtures. J. Phys. Organic Chem., 8: 617-625.
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  47. Wenkert, E., T.S. Arrhenius, B. Bookser, M. Guo and P. Mancini, 1990. Synthesis of. alpha.-(halomethyl) cycloalkanones. J. Organic Chem., 55: 1185-1193.
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  48. Nudelman, N.S., P.M. Mancini, R.D. Martinez and L.R. Vottero, 1987. Solvents effects on aromatic nucleophilic substitutions. Part 5. Kinetics of the reactions of 1-fluoro-2, 4-dinitrobenzene with piperidine in aprotic solvents. J. Chem. Soc. Perkin Trans., 2: 951-954.
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  49. Martinez, R.D., P.M. Mancini, L.R. Vottero and N.S. Nudelman, 1986. Solvent effects on aromatic nucleophilic substitutions. Part 4. Kinetics of the reaction of 1-chloro-2, 4-dinitrobenzene with piperidine in protic solvents. J. Chem. Soc. Perkin Trans., 2: 1427-1431.
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  50. Mancini, P.M., R.D. Martinez, L.R. Vottero and N.S. Nudelman, 1984. Solvent effects on aromatic nucleophilic substitutions. Part 3. The kinetics of the reaction of 2, 4-dinitrochlorobenzene with piperidine in aprotic solvents. J. Chem. Soc. Perkin Trans., 2: 1133-1138.
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