christiantantardini

Christian Tantardini

PhD Student

Ph.D. thesis title: “Towards Understanding High-Pressure Chemistry”

Supervisor: Prof. Artem R. Oganov

IDC committee members: Prof. Artem R. Oganov, Prof. Alexander Shapeev, Prof. Andriy Zhugayevych

Christian obtained his Bachelor’s Degree in Chemistry and Industrial Chemistry. University of Study of INSUBRIA, Como (Italy). He was graduated with 110/110 and it was obtained in only 2 years with thesis title: “Tunnel Effect in Carbon Nanotubes – Simplified Models”. Supervisor was Dr. Massimo Mella. Christian continued his studies in Milano where he obtained Master of Science in Chemistry at University of Milano, Milano (Italy). He was graduated with 110/110 and praise with thesis title: “Development of novel topological tools for the real space investigation of spin density in organometallic complexes”. Supervisors were Dr. Leonardo Lo Presti and Dr. Carlo Gatti. After that, Christian spent his first of PhD study at the Novosibirsk State University under supervision of Prof. Elena V. Boldyreva focusing in the Theoretical field of Charge Density with different approaches in Quantum Chemical Topology. During this time he developed Bader’s Theory and applied to solve specific problem in solid sate matter as in gas phase. Furthermore, in the 2018 Christian transferred his PhD into SkolTech under supervision of Prof. Artem R. Oganov is searching to explain the chemical bond at high pressure being seen in literature that the application of high pressure (hundreds of gigapascals) to materials, besides modifying their properties changes dramatically their reactivity.

List of papers:

  1. Christian Tantardini, Davide Ceresoli, Enrico Benassi. Source Function and Plane Waves: Toward Complete Bader Analysis. Journal of Computational Chemistry (2016), DOI: 10.1002/jcc.24433.
  2. Christian Tantardini, Sergey G. Arkhipov, Ksenya A. Cherkashina, Alexander S. Kil’met’eva and Elena V. Boldyreva. Crystal structure of a 2:1 co-crystal of meloxicam with acetylendicarboxylic acid. Acta Cryst E (2016), DOI: https://doi.org/10.1107/S2056989016018909.
  3. Christian Tantardini, Elena V. Boldyreva, and Enrico Benassi. Hypervalency in Organic Crystals: A Case Study of the Oxicam Sulfonamide Group. J. Phys. Chem. A (2016), DOI: 10.1021/acs.jpca.6b10703.
  4. Christian Tantardini, Enrico Benassi. Topology vs Thermodynamics in Chemical Reactions: The Instability of PH5. Phys. Chem. Chem. Phys. (2017), DOI: 10.1039/C7CP06130G.
  5. Christian Tantardini, Enrico Benassi. Crystal Structure Resolution of an Insulator Due to Cooperative Jahn-Teller through Bader’s Theory: The Challenging Case of Cobaltite Oxide Y114. Dalton Transaction (2018), DOI: 10.1039/C8DT00073E.
  6. Christian Tantardini. A new equation for real gases developed into the framework of Bader’s Theory. Theoretical Chemistry Accounts (2018), DOI: 10.1007/s00214-018-2271-7.
  7. Christian Tantardini, Sergey G. Arkipov, Kseniya A. Cherkashina, Alexander S. Kil’met’ev, Elena V. Boldyreva. Synthesis and crystal structure of a meloxicam co-crystal with benzoic acid. Structural Chemistry (2018), DOI: 10.1007/s11224-018-1166-5.
  8. Christian Tantardini, Adam A. L. Michalchuk Dess‐martin periodinane: The reactivity of a λ5‐iodane catalyst explained by topological analysis. International Journal of Quantum Chemistry (2018), DOI: 10.1002/qua.25838.
  9. Christian Tantardini. When does a hydrogen bond become a van der Waals interaction? a topological answer. Journal of Computational Chemistry (2019), DOI: 10.1002/jcc.25774.
  10. Alexey Yu. Fedorov, Tatiana N. Drebushchak, Christian Tantardini. Seeking the best model for non-covalent interactions within the crystal structure of meloxicam. Computational and Theoretical Chemistry (2019), DOI: 10.1016/j.comptc.2019.04.012.

 

Front Cover:

  1. Christian Tantardini, Davide Ceresoli, Enrico Benassi. Source Function and Plane Waves: Toward Complete Bader Analysis. Journal of Computational Chemistry (2016), DOI: 10.1002/jcc.24459.
  2. Christian Tantardini, Adam A. L. Michalchuk Dess‐martin periodinane: The reactivity of a λ5‐iodane catalyst explained by topological analysis. International Journal of Quantum Chemistry (2018), DOI: 10.1002/qua.25838. DOI: 10.1002/qua.25905.
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