{"id":345,"date":"2018-03-05T11:56:13","date_gmt":"2018-03-05T10:56:13","guid":{"rendered":"http:\/\/convegni.unica.it\/iccst-14\/?page_id=345"},"modified":"2019-06-04T06:57:07","modified_gmt":"2019-06-04T04:57:07","slug":"scientific-program","status":"publish","type":"page","link":"https:\/\/convegni.unica.it\/iccst-14\/scientific-program\/","title":{"rendered":"Scientific Program"},"content":{"rendered":"

\"\"<\/p>\n

“Rada di S. Efisio” Nora (7 Km from the Conference Venue)<\/em><\/p>\n

\"\"ICCST-14 Scientific Program
\n<\/strong><\/p>\n

ICCST-14 Scientific Program at a glance<\/a><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

June 3, 2019 (Monday)<\/strong><\/p>\n

16:30\u00a0\u00a0 <\/strong>Registration<\/p>\n

19:30<\/strong>\u00a0\u00a0 Welcome Party<\/p>\n

____________________________________________________________<\/strong><\/p>\n

June 4, 2019 (Tuesday)<\/strong><\/p>\n

8:45-9:00\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong>Opening<\/p>\n

Session 1<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Claudio Santi<\/u><\/em><\/p>\n

9:00-9:35<\/strong><\/p>\n

PL1<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Thomas G. Back (University of Calgari, Canada)<\/p>\n

Redox Properties of Organoselenium Compounds in Biology and Beyond<\/em><\/strong><\/p>\n

 <\/p>\n

9:35-10:00<\/strong><\/p>\n

IL1<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Sangit Kumar (Indian Institute of Science Education and Research (IISER) Bhopal, India)<\/p>\n

Organochalcogens: Synthesis, Antioxidant and Oxidant Biological Catalytic Activities<\/em><\/strong><\/p>\n

 <\/p>\n

10:00-10:25<\/strong><\/p>\n

IL2<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Ludger A. Wessjohann (Leibniz Institute of Plant Biochemistry (IPB), Germany)<\/p>\n

Synthetic, Medicinal and Analytic Studies on Organoselenides: Multi Component Reactions, Redox and Cancer Properties & Proteomics<\/em><\/strong><\/p>\n

 <\/p>\n

10.25-10.40<\/strong><\/p>\n

OC1<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Thomas Junk (University of Louisiana at Lafayette, USA)<\/p>\n

Novel Organotellurium Heterocycles Derived from Bis(2-Aminophenyl)ditelluride<\/em><\/strong><\/p>\n

 <\/p>\n

10:40-11:10<\/strong> Coffee break<\/strong><\/p>\n

\u00a0<\/u><\/strong><\/p>\n

Session 2<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Toshiaki Murai <\/u><\/em><\/p>\n

11:10-11:35<\/strong><\/p>\n

IL3<\/strong> \u00a0\u00a0\u00a0\u00a0\u00a0 Stefano Menichetti (Universit\u00e0 degli Studi di Firenze, Italy)<\/p>\n

Selenium Nucleophiles and Sulfur Electrophiles: An Exciting Synthetic Combination<\/em><\/strong><\/p>\n

\u00a0<\/em><\/p>\n

11:35-12:00<\/strong><\/p>\n

IL4<\/strong> Thomas Wirth (Cardiff University, U.K.)<\/p>\n

Selenoorganic Chemistry and Beyond<\/em><\/strong><\/p>\n

\u00a0<\/em><\/p>\n

12:00-12:25<\/strong><\/p>\n

IL5<\/strong> Ignacio Vargas-Baca (<\/em>McMaster University, Hamilton, Canada)<\/em><\/p>\n

Expanding the Supramolecular Chemistry of<\/strong><\/em> iso-Chalcogenazole<\/em><\/strong> N-oxides<\/strong><\/em><\/p>\n

\u00a0<\/em><\/p>\n

12:25-12:40<\/strong><\/p>\n

OC2<\/strong> Gianluca Ciancaleoni (Universit\u00e0 degli Studi di Pisa, Italy)<\/p>\n

Influence of Weak Interactions on the Selenium Bonding and Reactivity<\/em><\/strong><\/p>\n

\u00a0<\/em><\/p>\n

12:40-12:55<\/strong><\/p>\n

OC3\u00a0\u00a0\u00a0\u00a0 <\/strong>Torubaev Yury V. (N.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, <\/em>Russia)<\/p>\n

Halogen and Chalcogen Bonding in the Co-crystals of Organotellurides<\/em><\/strong><\/p>\n

 <\/p>\n

12:55-14:15 <\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Lunch<\/strong><\/p>\n

 <\/p>\n

Session 3<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. John F. Corrigan<\/u><\/em><\/p>\n

14:15-14:50<\/strong><\/p>\n

PL2<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 John G. Brennan (Rutgers, The State University of New Jersey, USA)<\/p>\n

Lanthanides and Actinides with S\/Se\/Te: Molecules, Nanoscale Clusters, and Solid-State Materials<\/em><\/strong><\/p>\n

 <\/p>\n

14:50-15:15<\/strong><\/p>\n

IL6<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Jens Beckmann (University of Bremen, Germany)<\/p>\n

Through-Space Interactions between Phosphorus and Tellurium in peri-Substituted Scaffolds<\/em><\/strong><\/p>\n

 <\/p>\n

15:15-15:40<\/strong><\/p>\n

IL7<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Risto S. Laitinen (University of Oulu, Finland)<\/p>\n

Chalcogen-Chalcogen Secondary Bonding Interactions<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

15:40-15:55<\/strong><\/p>\n

OC4\u00a0\u00a0\u00a0\u00a0 <\/strong>Wolfgang Weigand (Friedrich-Schiller-Universit\u00e4t Jena, Germany)<\/p>\n

Macrocyclic Polytelluroethers \u2013 Synthesis and Coordination Chemistry<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

15:55-16:10<\/strong><\/p>\n

OC5\u00a0\u00a0\u00a0\u00a0 <\/strong>Harkesh B. Singh (Indian Institute of Technology Bombay, India)<\/p>\n

Organotellurium Cations and Telluroxanes Stabilized by Intramolecular Coordination<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

16:10-16:30<\/strong> Coffee break<\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

Session 4<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Diego Alves<\/u><\/em><\/p>\n

16:30-16:45<\/strong><\/p>\n

OC6<\/strong>\u00a0\u00a0\u00a0\u00a0 Mariola Zieli\u0144ska-B\u0142ajet (Wroc\u0142aw University of Science and Technology, Poland)<\/p>\n

Selenoureas. New Cinchona Alkaloid Derivatives as Bifunctional Organocatalysts<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

16:45-17:00<\/strong><\/p>\n

OC7<\/strong>\u00a0\u00a0\u00a0\u00a0 Jos\u00e9 G Fern\u00e1ndez-Bola\u00f1os (Universidad de Seville, Spain)<\/p>\n

Organoselenium Compounds as Anti-Alzheimer\u00b4s and <\/em>Antiproliferative Agents<\/em><\/p>\n

 <\/p>\n

17:00-17:15<\/strong><\/p>\n

OC8\u00a0\u00a0\u00a0\u00a0 <\/strong>Jacek \u015acianowski (Nicolaus Copernicus University in Torun, Poland)<\/p>\n

Organoselenium Compounds Decorated with Monoterpene Skeletons<\/em><\/strong><\/p>\n

 <\/p>\n

17:15-17:30<\/strong><\/p>\n

OC9\u00a0\u00a0\u00a0\u00a0 <\/strong>Francesca Marini (Universit\u00e0 di Perugia, Italy)<\/p>\n

A Selenone-mediated Multicomponent Strategy for the Synthesis of Spirooxindoles Derivatives<\/em><\/p>\n

\u00a0<\/em><\/p>\n

17:30-19:00<\/strong> Poster Session Program Poster Presentations (PP)<\/a> [Group Photo]
\n<\/strong><\/p>\n

____________________________________________________________<\/strong><\/p>\n

June 5, 2019 (Wednesday)<\/strong><\/p>\n

Session 5<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Gianluca Ciancaleoni<\/u><\/em><\/p>\n

8:45-9:20<\/strong><\/p>\n

PL3<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Govindasamy Mugesh (Indian Institute of Science, Bangalore, India)<\/p>\n

Selenium and Thyroid: Synthetic Organoselenium Compounds as Iodothyronine Deiodinase Mimetics <\/em><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

9:20-9:45 <\/strong><\/p>\n

IL8<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Norman Metanis (The Hebrew University of Jerusalem, Jerusalem, Israel)<\/p>\n

Selenium Chemistry as a Tool to Study Protein Science<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

9:45-10:10<\/strong><\/p>\n

IL9\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong>Huaping Xu (Tsinghua University, Beijing, P.R. China)<\/p>\n

Selenium-containing Polymer for Adaptive and Biomedical Materials<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

10.10-10.25<\/strong><\/p>\n

OC10<\/strong>\u00a0\u00a0\u00a0 Dwight Seferos (University of Toronto, Canada)<\/p>\n

Tellurium-Containing Conducting Polymers and Photocatalysts<\/em><\/strong><\/p>\n

 <\/p>\n

10.25-10.40<\/strong><\/p>\n

OC11\u00a0\u00a0 <\/strong>Andrey V. Zibarev (N.N. Vorozhtsov Institute of Organic Chemistry, Russian Academy of Sciences, Siberian Branch, Novosibirsk, Russia)<\/p>\n

Structurally Defined Radical Anions of 2,1,3-Benzochalcogenadiazoles<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

10:40-11:10<\/strong> Coffee break<\/strong><\/p>\n

 <\/p>\n

Session 6<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. <\/u><\/em>K. Indira Priyadarsini<\/u><\/em><\/p>\n

11:10-11:35<\/strong><\/p>\n

IL10<\/strong>\u00a0\u00a0\u00a0\u00a0 Michael J. Davies (University of Copenhagen, Denmark)<\/p>\n

Reaction of Selenium Compounds with Reactive Oxidants and the Control of Oxidative Stress<\/strong><\/em><\/p>\n

 <\/p>\n

11:35-12:00<\/strong><\/p>\n

IL11<\/strong>\u00a0\u00a0\u00a0\u00a0 Sougat Misra (Karolinska Institutet, Sweden)<\/p>\n

Unraveling the Potency of Two Simple Selenium Compounds as Experimental Cancer Chemotherapeutics<\/strong><\/em><\/p>\n

 <\/p>\n

12:00-12:25<\/strong><\/p>\n

IL12<\/strong>\u00a0\u00a0\u00a0\u00a0 Carl H. Schiesser (Seleno Therapeutics Pty Ltd, Brighton East, Australia)<\/p>\n

1,4-Anhydro-4-seleno-d-talitol<\/em><\/strong> (SeTal): A remarkable Selenium-containing Therapeutic Molecule<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

12:25-12:40<\/strong><\/em><\/p>\n

OC12\u00a0\u00a0\u00a0 <\/strong>Jing Su (Nanjing Tech University, Nanjing, P.R. China)<\/p>\n

Cancer Theranostic Platform Based upon Ferrocenylselenoethers<\/em><\/strong><\/p>\n

\u00a0<\/em><\/p>\n

12:40-12:55<\/strong><\/p>\n

OC13\u00a0\u00a0 <\/strong>Kei Goto (School of Science, Tokyo Institute of Technology, Japan)<\/p>\n

Synthesis and Reactions of Selenocysteine-Derived Selenenic Acids Stabilized by a Nano-Sized Molecular Cradle<\/em><\/strong><\/p>\n

 <\/p>\n

12:55-14:15 <\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Lunch<\/strong><\/p>\n

14:15-18:40 <\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Conference Excursion<\/strong><\/p>\n

____________________________________________________________<\/strong><\/p>\n

June 6, 2019 (Thursday)<\/strong><\/p>\n

Session 7<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof.<\/u> Eder J. Lenard<\/u><\/em>\u00e3o<\/u><\/em><\/p>\n

8:45-9:20<\/strong><\/p>\n

PL4<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Xiaodan Zhao (Sun Yat-Sen University, Guangzhou, P.R. China)<\/p>\n

Chiral Bifunctional Chalcogenide Catalysis for Enantioselective Electrophilic Trifluoromethylthiolation, Arylthiolation, and Chlorination<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

9:20-9:45<\/strong><\/p>\n

IL13\u00a0\u00a0\u00a0\u00a0 <\/strong>Thierry Billard (CNRS-University of Lyon, France)<\/p>\n

Merging of Fluorinated Groups and Selenium: Why? How?<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

9:45-10:10<\/strong><\/p>\n

IL14\u00a0\u00a0\u00a0\u00a0 <\/strong>Toshiaki Murai (Gifu University, Japan)<\/p>\n

New Molecular Tools: Phosphorochalcogenoic Acid Derivatives Having a Binaphthyl Group<\/strong><\/em><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

10:10-10:25<\/strong><\/p>\n

OC14\u00a0\u00a0 <\/strong>Vimal K. Jain (UM-DAE Centre for Excellence in Basic Sciences, Mumbai, India)<\/p>\n

Pyridyl and Pyrimidyl Chalcogenolates of Coinage Metals and Their Utility as Molecular Precursors for the Preparation of Metal Chalcogenides<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

10:25-10:40<\/strong><\/p>\n

OC15\u00a0\u00a0 <\/strong>Cristian Silvestru (Babe\u015f-Bolyai University, Cluj-Napoca, Romania)<\/p>\n

Main Group Heavy Metal Compounds Containing Tetraphenylimidodiselenodiphosphinato Ligand<\/em><\/strong><\/p>\n

 <\/p>\n

10:40-11:10<\/strong> Coffee break<\/strong><\/p>\n

 <\/p>\n

Session 8<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Thomas Wirth<\/u><\/em><\/p>\n

11:10-11:35<\/strong><\/p>\n

IL15<\/strong>\u00a0\u00a0\u00a0\u00a0 Alexandre Breder (Georg-August-Universit\u00e4t G\u00f6ttingen, Germany)<\/p>\n

Light-Driven Selenium-<\/strong><\/em>\u03c0<\/strong><\/em>-Acid Catalysis \u2013 From Concepts to Applications<\/strong><\/em><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

11:35-12:00<\/strong><\/p>\n

IL16\u00a0\u00a0\u00a0\u00a0 <\/strong>Vladimir A. Potapov (A. E. Favorsky Institute of Chemistry Russian Academy of Sciences, Siberian Branch, Irkutsk, Russia)<\/p>\n

Efficient Regio- and Stereo-selective Approaches to Novel Families of Organochalcogen Functionalized Compounds Based on Electrophilic Selenium- and Tellurium-containing Reagents<\/strong><\/em><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

12:00-12:25<\/strong><\/p>\n

IL17<\/strong> \u00a0\u00a0\u00a0 <\/strong>Eder Jo\u00e3o Lenard\u00e3o (<\/em>Universidade Federal de Pelotas, Brazil)<\/em><\/p>\n

New Strategies to Prepare Chalcogen-functionalized Heterocycles<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

12:25-12:40<\/strong><\/p>\n

OC16\u00a0\u00a0 <\/strong>Lukas Vogel (Ruhr-University Bochum, Germany)<\/p>\n

Multidentate Chalcogen Bond Donors in Organic Synthesis<\/em><\/strong><\/p>\n

\u00a0<\/em><\/p>\n

12:40-12:55<\/strong><\/p>\n

OC17\u00a0\u00a0 <\/strong>Nicolas Biot (Cardiff University, U.K<\/em>.)<\/p>\n

Programming Recognition Arrays Through double Chalcogen-Bonding Interactions<\/em><\/strong><\/p>\n

 <\/p>\n

12:55-14:15 <\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Lunch<\/strong><\/p>\n

 <\/p>\n

Session 9<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong><\/em>Chairman Prof. Norman Metanis<\/u><\/em><\/p>\n

14:15-14:50<\/strong><\/p>\n

PL5\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong>Michio Iwaoka (Tokai University, Hiratsuka, Japan)<\/p>\n

Weak Interaction Network at the Active Site of Selenoenzymes<\/strong><\/em><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

14:50-15:15<\/strong><\/p>\n

IL18\u00a0\u00a0\u00a0\u00a0 <\/strong>K. Indira Priyadarsini (Bhabha Atomic Research Centre, Mumbai, India)<\/p>\n

Free Radical Chemistry and In vivo Biological Studies of Diselenodipropionic acid (DSePA), a Selenocystine Derivative, as a Radiotherapy Adjuvant<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

15:15-15:40<\/strong><\/p>\n

IL19<\/strong>\u00a0\u00a0\u00a0\u00a0 Eufr\u00e2nio N. da Silva J\u00fanior (Federal University of Minas Gerais, Belo Horizonte, Brazil)<\/p>\n

Strategies towards Bioactive Quinoidal Molecules: Synthesis and Antitumor Activity of Selenium-containing Quinones<\/strong><\/em><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

15:40-15:55<\/strong><\/p>\n

OC18\u00a0\u00a0 <\/strong>Laura Orian (Universit\u00e0 degli Studi di Padova, Italy<\/em>)<\/p>\n

Aspects of the S\/Se\/Te Chemistry and Biochemistry of H2<\/sub>O2<\/sub> Reduction Disclosed in silico<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

15:55-16:10<\/strong><\/p>\n

OC19\u00a0\u00a0 <\/strong>Jason Shearer (Trinity University, San Antonio, USA)<\/p>\n

Subtle Differences in the Electronic Structure of the Nickel Selenocysteinate vs Cysteinate Bond Renders a Ni-Se Metallopeptide Functionally Inactive<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

16:10-16:30<\/strong> Coffee break<\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

Session 10<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Vimal K. Jain<\/u><\/em><\/p>\n

16:30-16:45<\/strong><\/p>\n

OC20\u00a0\u00a0 <\/strong>Norio Nakata (Saitama University, Japan)<\/p>\n

16-Electron Selenairidacycle: Synthesis, Structure, and Reactivity<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

16:45-17:00<\/strong><\/p>\n

OC21\u00a0\u00a0 <\/strong>Yuichiro Mutoh (Tokyo University of Science, Japan)<\/p>\n

Synthesis and Properties of Cationic Ruthenium Chalcogenocarbonyl Complexes with a Half-sandwich Structure<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

17:00-17:15<\/strong><\/p>\n

OC22\u00a0\u00a0 <\/strong>Bekington Myrboh (North Eastern Hill University, Shillong, India)<\/p>\n

Selenium Dioxide Mediated <\/em><\/strong>Reaction of Aryl\/Alkyl Methyl Ketones with Aliphatic\/Aromatic Alcohols Catalyzed by PTSA\u00b7H2<\/sub>O: A Simple and Convenient Protocol for Easy Access to a Library of \u03b1<\/em><\/strong>–<\/em><\/strong>Ketoacetals<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

17:15-17:30<\/strong><\/p>\n

OC23\u00a0\u00a0 <\/strong>Jian Zhu (Soochow University, Suzhou, P.R. China)<\/p>\n

Seleno-Mediated Living Radical Polymerization (Se-LRP): from Fundamental to Application<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

17:30-17:45<\/strong><\/p>\n

OC24\u00a0\u00a0 <\/strong>Rohit Singh Chauhan (K.J. Somaiya College of Science and Commerce, Mumbai, India)<\/p>\n

Reactivity of Hemilabile Organochalcogen Ligands Towards Group 10 metal Precursors <\/em><\/strong>[MCl2<\/sub>(L<\/em><\/strong>–<\/em>L)]<\/em><\/strong> (<\/em><\/strong>L<\/em><\/strong>–<\/em>L = PPh3<\/sub>, dppm, dppe, dppp; M = Ni, Pd, Pt)<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

Session 11<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. <\/u><\/em>Eufr\u00e2nio N. da Silva J\u00fanior<\/u><\/em><\/p>\n

17:45-19:00<\/strong><\/p>\n

S<\/strong>HORT ORAL COMMUNICATIONS<\/strong> (SOC) Program SOC<\/a>
\n<\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

20:00 GALA DINNER <\/strong><\/p>\n

___________________________________________________<\/strong><\/em>_____________________________<\/strong><\/em><\/p>\n

June 7, 2019 (Friday)<\/strong><\/p>\n

Session 12<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Jens Beckmann<\/u><\/em><\/p>\n

8:45-9:20<\/strong><\/p>\n

PL6<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Gillian Reid (University of Southampton, U.K.)<\/p>\n

Chalcogenoether and Chalcogenolate Complexes as Single Source Precursors for Functional Semiconducting Thin Film Materials<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

9:20-9:45<\/strong><\/p>\n

IL20<\/strong>\u00a0\u00a0\u00a0\u00a0 John F. Corrigan (<\/em>The University of Western Ontario, London, Ontario, Canada)<\/em><\/p>\n

N-Heterocyclic Carbene-Stabilized Metal-ESiMe3<\/sub> Complexes (E = S, Se, Te): Precursors to Coinage Metal-Chalcogenide Clusters with Tunable Optical Properties<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

9:45-10:10<\/strong><\/p>\n

IL21\u00a0\u00a0\u00a0\u00a0 <\/strong>Yasumitsu Ogra (Chiba University, Japan)<\/p>\n

Mechanisms Underlying Selenium Methylation for Urinary Excretion as Trimethylselenonium<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/em><\/p>\n

10:10-10:25<\/strong><\/p>\n

OC25\u00a0\u00a0 <\/strong>Fabian Mohr (Bergische Universit\u00e4t Wuppertal, Germany)<\/p>\n

Copper(I) and Gold(I) Carbene Complexes with Selenourea Ligands<\/em><\/strong><\/p>\n

 <\/p>\n

10:25-10:40<\/strong><\/p>\n

OC26\u00a0\u00a0 <\/strong>Anca Silvestru (Babe\u015f-Bolyai University, Cluj-Napoca, Romania)<\/p>\n

Organochalcogen Compounds as Multidentate Ligands: Synthesis, Structure and Applications<\/em><\/strong><\/p>\n

 <\/p>\n

10:40-11:10<\/strong> Coffee break<\/strong><\/p>\n

 <\/p>\n

Session 13<\/u><\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Vito Lippolis<\/u><\/em><\/p>\n

11:10-11:25<\/strong><\/p>\n

OC27\u00a0\u00a0 <\/strong>Katarzyna Bierla (<\/em>Institute of Analytical Sciences (IPREM), Centre National de la Recherche Scientifique, (UMR5254, CNRS-UPPA), Pau, France)<\/em><\/p>\n

Metodological Developments for Selenometabolite Speciation in Animal Tissues<\/em><\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

11:25-11:40<\/strong><\/p>\n

OC28\u00a0\u00a0 <\/strong>Mao Minoura (Rikkyo University, Tokyo, Japan)<\/p>\n

Synthesis and Structure of Tetraaryltellurium(IV)<\/em><\/strong><\/p>\n

 <\/p>\n

11:40-11:55<\/strong><\/p>\n

OC29\u00a0\u00a0 <\/strong>Xiangqiang Pan (<\/em>Soochow University, Suzhou, P.R. China)<\/em><\/p>\n

Synthesis and Application of Se-containing Polymers<\/em><\/strong><\/p>\n

 <\/p>\n

11:55-12:10<\/strong><\/p>\n

OC30\u00a0\u00a0 <\/strong>Saulius Klima\u0161auskas (<\/em>Vilnius University, Lithuania)<\/em><\/p>\n

Targeted Incorporation of Selenium for Improved Analysis of Nucleic Acids and Proteins<\/em><\/strong><\/p>\n

 <\/p>\n

12:10-12:45<\/strong><\/p>\n

PL7<\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0 Antonio L. Braga (Universidade Federal de Santa Catarina, Florianop\u00f3lis, Brazil)<\/p>\n

Use of Halogen Species in C-H Bond Chalcogenation via Sustainable Approach<\/strong><\/em><\/p>\n

\u00a0<\/em><\/p>\n

12:45-12:55<\/strong><\/p>\n

Closing Remarks<\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

12:55-14:15 <\/strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Lunch<\/strong><\/p>\n

________________________________________________________________________________<\/strong><\/p>\n

\u00a0<\/strong><\/p>\n

 <\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

“Rada di S. Efisio” Nora (7 Km from the Conference Venue) ICCST-14 Scientific Program ICCST-14 Scientific Program at a glance \u00a0 June 3, 2019 (Monday) 16:30\u00a0\u00a0 Registration 19:30\u00a0\u00a0 Welcome Party ____________________________________________________________ June 4, 2019 (Tuesday) 8:45-9:00\u00a0\u00a0\u00a0\u00a0\u00a0 Opening Session 1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Chairman Prof. Claudio Santi 9:00-9:35 PL1\u00a0\u00a0\u00a0\u00a0\u00a0 Thomas G. Back (University of Calgari, Canada) Redox Properties of Organoselenium Compounds in Biology and Beyond   9:35-10:00 IL1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Sangit Kumar (Indian Institute of Science Education and Research (IISER) Bhopal, India) Organochalcogens: Synthesis, Antioxidant and Oxidant Biological Catalytic Activities   10:00-10:25 IL2\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Ludger A. Wessjohann (Leibniz Institute of Plant Biochemistry (IPB), Germany) Synthetic, Medicinal and […]<\/a><\/p>\n","protected":false},"author":2527,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-345","page","type-page","status-publish","hentry","post-seq-1","post-parity-odd","meta-position-corners","fix"],"_links":{"self":[{"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/pages\/345","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/users\/2527"}],"replies":[{"embeddable":true,"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/comments?post=345"}],"version-history":[{"count":23,"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/pages\/345\/revisions"}],"predecessor-version":[{"id":874,"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/pages\/345\/revisions\/874"}],"wp:attachment":[{"href":"https:\/\/convegni.unica.it\/iccst-14\/wp-json\/wp\/v2\/media?parent=345"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}