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Jaroslav V. Burda

Researcher at Charles University in Prague

Publications -  110
Citations -  3474

Jaroslav V. Burda is an academic researcher from Charles University in Prague. The author has contributed to research in topics: Ab initio & Density functional theory. The author has an hindex of 32, co-authored 108 publications receiving 3269 citations. Previous affiliations of Jaroslav V. Burda include Czechoslovak Academy of Sciences & Sewanee: The University of the South.

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Density functional study of structural and electronic properties of bimetallic silver–gold clusters: Comparison with pure gold and silver clusters

TL;DR: In this article, the authors have determined structures, ionization potentials, and vertical detachment energies for neutral and charged bimetallic AgmAun[3⩽(m+n)⵽5] clusters.
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Interaction of DNA Base Pairs with Various Metal Cations (Mg2+, Ca2+, Sr2+, Ba2+, Cu+, Ag+, Au+, Zn2+, Cd2+, and Hg2+): Nonempirical ab Initio Calculations on Structures, Energies, and Nonadditivity of the Interaction

TL;DR: In this paper, the interaction of adenine−thymine and guanine−cytosine base pairs with various metal cations (Mg2+,..., Hg2+) was studied by nonempirical ab initio methods with inclusion of correlation energy.
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Ab Initio Study of the Interaction of Guanine and Adenine with Various Mono- and Bivalent Metal Cations (Li+, Na+, K+, Rb+, Cs+; Cu+, Ag+, Au+; Mg2+, Ca2+, Sr2+, Ba2+; Zn2+, Cd2+, and Hg2+)

TL;DR: The interaction of guanine and adenine with ions of groups Ia, Ib, IIa, IIb were studied at the Hartree−Fock and second-order Moller−Plesset levels employing all-electron (AE) and pseudopotential treatmetns.
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Interaction between the Guanine−Cytosine Watson−Crick DNA Base Pair and Hydrated Group IIa (Mg2+, Ca2+, Sr2+, Ba2+) and Group IIb (Zn2+, Cd2+, Hg2+) Metal Cations

TL;DR: In this paper, the structure and energy properties of the guanine−cytosine Watson−Crick DNA base pair and pentahydrated Mg2+, Ca2+, Sr2+, Ba2+, Zn2+, Cd2+, and Hg2+ metal cations were studied.
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Anthracyclines and ellipticines as DNA-damaging anticancer drugs: recent advances.

TL;DR: Therapies utilizing the antineoplastic activities of anthracyclines and ellipticines combined with novel strategies such as nanotechnologies for safer drug delivery, as well as strategies based on gene therapy, could significantly contribute to medical practice.