{"id":4,"date":"2014-10-14T13:20:20","date_gmt":"2014-10-14T13:20:20","guid":{"rendered":"http:\/\/medicina.udd.cl\/centro-quimica-medica\/?post_type=person&#038;p=4"},"modified":"2022-04-12T14:03:28","modified_gmt":"2022-04-12T14:03:28","slug":"paola-campodonico","status":"publish","type":"person","link":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/persona\/paola-campodonico\/","title":{"rendered":"Paola  Campod\u00f3nico, PhD."},"featured_media":173,"template":"","people_tax":[4045],"people_areas":[],"people_levels":[],"class_list":["post-4","person","type-person","status-publish","has-post-thumbnail","hentry","people_tax-integrantes"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Paola Campod\u00f3nico - Centro de Qu\u00edmica M\u00e9dica | UDD<\/title>\n<meta name=\"description\" content=\"Directora y profesor asociado del Centro de Qu\u00edmica M\u00e9dica de la Facultad de Medicina Cl\u00ednica Alemana Universidad del Desarrollo\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/medicina.udd.cl\/centro-quimica-medica\/persona\/paola-campodonico\/\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/medicina.udd.cl\/centro-quimica-medica\/persona\/paola-campodonico\/\",\"url\":\"https:\/\/medicina.udd.cl\/centro-quimica-medica\/persona\/paola-campodonico\/\",\"name\":\"Paola Campod\u00f3nico - 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Qu\u00edmico, Universidad de Santiago de Chile. Doctor en Ciencias menci\u00f3n Qu\u00edmica, Pontificia Universidad Cat\u00f3lica de Chile. <\/p>\n\t\t\t\t\t\t\t\t\t\t<p>&nbsp;<\/p>\n<p><strong>CARGO ACTUAL:<\/strong><\/p>\n<p>Directora del Centro de Qu\u00edmica M\u00e9dica.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>DOCENCIA:<\/strong><\/p>\n<p>Coordinadora y Docente del curso de Qu\u00edmica General y Qu\u00edmica Org\u00e1nica de la carrera de Medicina. En \u00e9ste, la Dra. Campod\u00f3nico se desempe\u00f1a como Profesor de C\u00e1tedra, Trabajos Pr\u00e1cticos y de Talleres de C\u00e1tedra.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>INVESTIGACI\u00d3N:<\/strong><\/p>\n<p>La Dra. Campod\u00f3nico realiza investigaci\u00f3n en efectos del medio de polaridad variable.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>PROYECTOS EN EJECUCI\u00d3N:<\/strong><\/p>\n<ul>\n<li>Experimental &amp; theoretical studies on nucleophilic substitution reactions in solvents of varying polarity. Investigador Responsable. Proyecto Fondecyt Regular # 1150759. Cl\u00ednica Alemana-Universidad del Desarrollo<\/li>\n<li>Iniciativa Cient\u00edfica Milenio RC-130006 CILIS: Centro Interdisciplinario de L\u00edquidos I\u00f3nicos. Investigador Asociado.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>PUBLICACIONES CON AFILIACI\u00d3N DEL CENTRO:<\/strong><\/p>\n<ul>\n<li><strong>Site activation effects promoted by intramolecular hydrogen bond interactions in snar reactions.<\/strong>\u00a0Sebastian Gallardo-Fuentes, Ricardo A. Tapia, Renato Contreras and Paola R. Campod\u00f3nico. RSC Advances, 4, 30638, 2014.<\/li>\n<li><strong>Mechanistic pathways in aromatic nucleophilic substitution in conventional solvents and ionic liquids.\u00a0<\/strong>Marcela Gazit\u00faa, Ricardo A. Tapia, Renato Contreras and Paola R. Campod\u00f3nico.\u00a0New Journal of Chemistry, 38, 2611, 2014.<\/li>\n<li><strong>Changes in the SNAr reaction mechanism brought about by preferential solvation.\u00a0<\/strong>Jazm\u00edn Alarc\u00f3n-Esp\u00f3sito, Ricardo A. Tapia, Renato Contreras and Paola R. Campod\u00f3nico. RSC Adv., 2015, 5, 99322\u201399328<\/li>\n<li><strong>Ionic Liquids binary mixtures: how different factors contribute to determine their effect on the reactivity.<\/strong>\u00a0Salvatore Marullo, Francesca D\u2019Anna , Paola R. Campodonico and Renato Noto\u00a0RSC Adv., 2016, 6, 90165<\/li>\n<li><strong>Gutmann\u2019s Donor Numbers Correctly Assess the Effect of the Solvent on the Kinetics of SNAr Reactions in Ionic Liquids.<\/strong>\u00a0Jazm\u00edn Alarc\u00f3n-Esp\u00f3sito, Renato Contreras, Ricardo A. Tapia, and Paola R. Campod\u00f3nico. Chem. Eur. J. 2016, 22, 13347 \u2013 13351<\/li>\n<li>Cap\u00edtulo de libro: T\u00edtulo Libro:<strong> Arene Chemistry: Reaction Mechanisms and Methods for Aromatic Compounds.<\/strong> T\u00edtulo Cap\u00edtulo: <strong>Computational and Experimental Methods for Predicting Reaction Mechanisms in Nucleophilic Aromatic Substitutions.\u00a0<\/strong>Autores: Renato Contreras, Rodrigo Ormaz\u00e1bal-Toledo, Paola R. Campod\u00f3nico.\u00a0Editorial: John Wiley &amp; Sons.\u00a0Editor: Jacques Mortier<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>PUBLICACIONES PREVIAS:<\/strong><\/p>\n<ul>\n<li><strong>Kinetic and theoretical study on nucleofugality in the phenolysis of 3-nitrophenyl and 4-nitrophenyl 4-cyanophenyl thionocarbonates.<\/strong>\u00a0Enrique A. Castro, \u00c1lvaro Ca\u00f1ete, Paola R. Campod\u00f3nico, Marjorie Cepeda, Paulina Pavez, Renato Contreras and Jos\u00e9 G. Santos. Chemical Physics Letters, 572, 130, 2013.<\/li>\n<li><strong>Hydrogen bond contribution to preferential solvation in snar reactions.\u00a0<\/strong>Rodrigo Ormaz\u00e1bal-Toledo, Jos\u00e9 G. Santos, Paulina R\u00edos, Enrique A. Castro, Renato Contreras, Paola R. Campod\u00f3nico. The Journal of Physical Chemistry B, 117, 5908, 2013<\/li>\n<li><strong>Specific nucleophile-electrophile interactions in nucleophilic aromatic substitutions.<\/strong>\u00a0Rodrigo Ormaz\u00e1bal-Toledo, Renato Contreras, Ricardo A. Tapia and \u00a0Paola R. Campod\u00f3nico. Organic and Biomolecular Chemistry, 11, 2302, 2013<\/li>\n<li><strong>Reactivity indices profile: a companion tool of the potential energy surfaces for the analysis of reaction mechanisms. Nucleophilic aromatic substitution.\u00a0<\/strong>Rodrigo Ormaz\u00e1bal-Toledo, Renato Contreras and \u00a0Paola R. Campod\u00f3nico. The Journal of Organic Chemistry, 78, 1091, 2013<\/li>\n<li><strong>Predicting the reaction mechanism of nucleophilic substitutions at carbonyl and thio-carbonyl centre.\u00a0<\/strong>Rodrigo Ormaz\u00e1bal-Toledo, Enrique A. Castro, Jos\u00e9 G. Santos, Daniela Mill\u00e1n, \u00c1lvaro Ca\u00f1ete, Renato Contreras, Paola R. Campod\u00f3nico. Journal of Physical Organic Chemistry, 25, 1359, 2012.<\/li>\n<li><strong>Are electrophilicity and electrofugality related concepts? a density functional theory study.\u00a0<\/strong>Rodrigo Ormaz\u00e1bal-Toledo, Paola R. Campod\u00f3nico, Renato Contreras. Organic Letters, 13, 822, 2011<\/li>\n<li><strong>Reactions of aryl acetates with secondary alicyclic amines in ethanol\/water mixtures: effect of the solvent composition on the kinetics and mechanism.<\/strong>\u00a0Enrique A. Castro, Daniela Mill\u00e1n, Raul Aguayo, Paola R. Campod\u00f3nico, Jos\u00e9 G. Santos. International Journal of Chemical Kinetics, 43, 687, 2011<\/li>\n<li><strong>Permanent group effect on nucleofugality in aryl benzoates.<\/strong>\u00a0Paola R. Campod\u00f3nico, Rodrigo Ormaz\u00e1bal-Toledo, Arie Aizman and Renato Contreras. Chemical Physics Letters, 498, 221, 2010<\/li>\n<li><strong>Reactivity of benzohydrazide derivatives towards acetylation reaction. Experimental and theoretical studies.<\/strong>\u00a0Paola R. Campod\u00f3nico, Margarita Aliaga, Jos\u00e9 G. Santos, Enrique A. Castro and Renato Contreras. Chemical Physics Letters, 488, 86, 2010<\/li>\n<li><strong>Experimental and theoretical studies on the nucleofugality patters in the aminolysis and phenolysis of s- aryl o-aryl thiocarbonates.\u00a0<\/strong>Enrique A. Castro, Margarita Aliaga, Paola R. Campod\u00f3nico, Marjorie Cepeda, Renato Contreras and Jos\u00e9 G. Santos. Journal of Organic Chemistry, 74, 9173, 2009<\/li>\n<li><strong>Electrophilicity of quinones and its relationships with hydride affinity.<\/strong>\u00a0Paola R. Campod\u00f3nico, Arie Aizman and Renato Contreras. Chemical Physics Letters, 471, 168, 2009<\/li>\n<li><strong>Proton-transport catalysis in intramolecular rearrangements. a density functional theory study.<\/strong>\u00a0Paola R. Campod\u00f3nico, Juan Andr\u00e9s, Arie Aizman and Renato Contreras. Chemical Physics Letters 464, 271, 2008<\/li>\n<li><strong>Structure-activity relationships for electrophilic sugars in interactions with nucleophilic biological target.<\/strong>\u00a0Paola R. Campod\u00f3nico and Renato Contreras. Bioorganic and Medicinal chemistry, 16, 3184, 2008<\/li>\n<li><strong>Reactions of aryl chlorothioformates with quinuclidines. a kinetic study.\u00a0<\/strong>Enrique. A. Castro, Margarita Aliaga, Paola R. Campod\u00f3nico, Jos\u00e9. R. Leis, Luis Garc\u00eda-R\u00edo, and Jos\u00e9 G. Santos. Journal of Physical Organic Chemistry, 21, 102, 2008<\/li>\n<li><strong>Electrofugality index of benzhydryl derivatives.<\/strong>\u00a0Paola R. Campod\u00f3nico, Claudio P\u00e9rez, Margarita Aliaga, Marcela Gazit\u00faa and Renato Contreras. Chemical Physics Letters, 447, 375, 2007<\/li>\n<li><strong>Nucleofugality index in \u03b1-elimination reactions.\u00a0<\/strong>Paola R. Campod\u00f3nico, Arie Aizman, Juan Andr\u00e9s and Renato Contreras. Chemical Physics Letters, 439, 177, 2007<\/li>\n<li><strong>Group electrophilicity as a model of nucleofugality in nucleophilic substitution reactions.<\/strong>\u00a0Paola R. Campod\u00f3nico, Arie Aizman and Renato Contreras. Chemical Physics Letters, 42, 340, 2006<\/li>\n<li><strong>Empirical scale of nucleophilicity for substituted pyridines.<\/strong>\u00a0Paola R. Campod\u00f3nico, Arie Aizman and Renato Contreras. Chemical Physics Letters, 42, 204, 2006<\/li>\n<li><strong>Kinetics and mechanistic study of the reaction of aryl chloroformiates with quinuclidines.\u00a0<\/strong>Enrique A. Castro, Margarita Aliaga, Paola R. Campod\u00f3nico, Jos\u00e9 G. Santos, Jos\u00e9 R. Leis and Luis Garc\u00eda-R\u00edo. Journal of Physical Organic Chemistry, 19, 683, 2006<\/li>\n<li><strong>Experimental and theoretical study on the substitution reactions of aryl 2,4-dinitrophenyl carbonates with quinuclidines.<\/strong> Enrique A. Castro, Paola R. Campod\u00f3nico, R. Contreras, P. Fuentealba, Jos\u00e9 G. Santos, J. Ram\u00f3n Leis, Luis Garc\u00eda-R\u00edo, Jos\u00e9 A. S\u00e1ez, and Luis R. Domingo. Tetrahedron, 62, 2555, 2006<\/li>\n<li><strong>Relationships between the electrophilicity index and experimental rate coefficient for the aminolysis of thiolcarbonates and dithiocarbonates.\u00a0<\/strong>Paola R. Campod\u00f3nico, Patricio Fuentealba, Enrique Castro, Jos\u00e9 G. Santos and Renato Contreras. The Journal of Organic Chemistry, 70, 1754, 2005<\/li>\n<li><strong>Relationship betwwen nucleophilicity\/electrophilicity indicres reaction mechanisms for the nucleophilic substitution reactions of carbonyl and thiocarbonyl compounds.\u00a0<\/strong>Paola Campod\u00f3nico, Jos\u00e9 G. Santos, Juan Andr\u00e9s and Renato Contreras. \u00a0Journal of Physical Organic Chemistry, 17, 273, 2004<\/li>\n<li><strong>Kinetics and mechanism of the aminolysis of 4-methylphenyl and 4-chlorophenyl-2,4-dinitrophenyl carbonates in aqueous ethanol.\u00a0<\/strong>Enrique A. Castro, Paola Campod\u00f3nico, Alejandra Toro and Jos\u00e9 G. Santos.The Journal of Organic Chemistry, 68, 15, 5930, 2003<\/li>\n<li><strong>A theoretical study on the relationship between nucleophilicity and ionization potentials in solution phase.\u00a0<\/strong>Renato Contreras, Juan Andres, Vicente S. Safont, Paola R. Campod\u00f3nico, Jos\u00e9 G. Santos. The Journal of Physical Chemistry A. 107, 29, 5588, 2003<\/li>\n<li><strong>Exploratory study of the effect of polar solvents upon the partitioning of solvents in non-aqueous reverse micellar solution.\u00a0<\/strong>Juana J. Silver, Rub\u00e9n D. Falcone, N.M Correa, M.A. Biasutti, Elsa Abuin, Eduardo Lissi and Paola \u00a0Campodonico. Langmuir, 19, 6, 2067, 2003<\/li>\n<li><strong>Kinetics and mechanism of the aminolysis of methyl 4-nitrophenyl, methyl 2,4-dinitrophenyl and 2,4-dinitrophenyl carbonates.\u00a0<\/strong>Enrique A. Castro, Margarita Aliaga, Paola Campod\u00f3nico and J.G. Santos. The Journal of Organic Chemistry, 67, 25, 8911, 2002<\/li>\n<li><strong>Kinetics and mechanism of the aminolysis of 4-nitrophenyl and 2,4-dinitrophenyl 4-methylphenyl carbonate in aqueous ethanol.<\/strong>\u00a0Enrique A. Castro, M\u00f3nica And\u00fajar, Paola Campod\u00f3nico and Jos\u00e9 G. Santos. International Journal of Chemical Kinetics, 34, 309, 2002<\/li>\n<li><strong>Merocyanine-type dyes from barbituric acid derivatives.<\/strong>\u00a0Marcos Caroli, Paola Campod\u00f3nico, Elsa Abuin and J. Kossanyi. Spectrochimica Acta Part A., 57, 1183, 2001<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n\t\t<\/div>\n\t<\/div>\n<\/div>\n"},"identifier":"d7262e00393052d40f6f3aba0cae0e590d988e8b","has_credential":[],"given_name":"Paola ","family_name":"Campod\u00f3nico, PhD.","name":"Paola  Campod\u00f3nico, PhD.","job_title":"Directora e Investigadora Docente","telephone":"","note":"Licenciada en Qu\u00edmica, Universidad de Santiago de Chile. Qu\u00edmico, Universidad de Santiago de Chile. Doctor en Ciencias menci\u00f3n Qu\u00edmica, Pontificia Universidad Cat\u00f3lica de Chile. \r\n","im":"","_self_schedule":null,"_links":{"self":[{"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/people\/4","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/people"}],"about":[{"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/types\/person"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/media\/173"}],"wp:attachment":[{"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/media?parent=4"}],"wp:term":[{"taxonomy":"people_tax","embeddable":true,"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/people_tax?post=4"},{"taxonomy":"people_areas","embeddable":true,"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/people_areas?post=4"},{"taxonomy":"people_levels","embeddable":true,"href":"https:\/\/medicina.udd.cl\/centro-quimica-medica\/wp-json\/wp\/v2\/people_levels?post=4"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}