Dejan-Kresimir Bucar, Ph.D.
Affiliations: | 2010 | Chemistry | University of Iowa, Iowa City, IA |
Area:
supramolecular chemistry and materials scienceGoogle:
"Dejan-Kresimir Bucar"Mean distance: 10.77 | S | N | B | C | P |
Parents
Sign in to add mentor| Leonard R. MacGillivray | grad student | 2010 | University of Iowa | |
| (Crystal engineering of organic and metal-organic solids: Design, structure and properties.) | ||||
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Publications
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| Clout A, Buanz A, Pang Y, et al. (2020) Mechanistic in situ and ex situ studies of phase transformations in molecular co-crystals. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Royakkers J, Minotto A, Congrave DG, et al. (2019) Doubly Encapsulated Perylene Diimides: Effect of Molecular Encapsulation on Photophysical Properties. The Journal of Organic Chemistry |
| Benhamou L, Foster RW, Ward DP, et al. (2019) Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass Green Chemistry. 21: 2035-2042 |
| Hasa D, Marosa M, Bučar D, et al. (2019) Mechanochemical Formation and “Disappearance” of Caffeine–Citric-Acid Cocrystal Polymorphs Crystal Growth & Design. 20: 1119-1129 |
| Bučar D, Friščić T. (2019) Professor William Jones and His Materials Chemistry Group: Innovations and Advances in the Chemistry of Solids Crystal Growth & Design. 19: 1479-1487 |
| Corpinot MK, Bučar D. (2019) A Practical Guide to the Design of Molecular Crystals Crystal Growth & Design. 19: 1426-1453 |
| Leventis A, Royakkers J, Rapidis AG, et al. (2018) Highly Luminescent Encapsulated Narrow Bandgap Polymers Based on Diketopyrrolopyrrole. Journal of the American Chemical Society |
| Diez SJ, Eddleston MD, Arhangelskis M, et al. (2018) Crystallization at Solvent Interfaces Enables Access to a Variety of Cocrystal Polymorphs and Hydrates Crystal Growth & Design. 18: 3263-3268 |
| Bučar D. (2017) Engineering Molecular Crystals: Backbreaking, yet Gratifying Crystal Growth & Design. 17: 2913-2918 |
| Corpinot MK, Guo R, Tocher DA, et al. (2017) Are Oxygen and Sulfur Atoms Structurally Equivalent in Organic Crystals? Crystal Growth & Design. 17: 827-833 |