Ivan Prokeš

ORCID: 0000-0003-3896-8941
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Crystallography and molecular interactions
  • Metal complexes synthesis and properties
  • Ferrocene Chemistry and Applications
  • Organometallic Complex Synthesis and Catalysis
  • Lanthanide and Transition Metal Complexes
  • Supramolecular Chemistry and Complexes
  • Fluorine in Organic Chemistry
  • Molecular Sensors and Ion Detection
  • Chemical Synthesis and Analysis
  • Carbon dioxide utilization in catalysis
  • Magnetism in coordination complexes
  • Inorganic Fluorides and Related Compounds
  • Catalytic C–H Functionalization Methods
  • Chemical Reaction Mechanisms
  • Metal-Organic Frameworks: Synthesis and Applications
  • Glycosylation and Glycoproteins Research
  • Polymer composites and self-healing
  • Microwave-Assisted Synthesis and Applications
  • Synthesis and Catalytic Reactions
  • Mass Spectrometry Techniques and Applications
  • Vanadium and Halogenation Chemistry
  • Advanced NMR Techniques and Applications
  • Oxidative Organic Chemistry Reactions

University of Warwick
2013-2024

Coventry (United Kingdom)
2015-2018

University of Oxford
2006-2009

University of St Andrews
2002-2006

University College London
2006

University of Glasgow
2006

University of Exeter
2002-2006

Comenius University Bratislava
1994-1996

Cyclic adenosine diphosphate (ADP)–ribose (cADPR) isomers are signaling molecules produced by bacterial and plant Toll/interleukin-1 receptor (TIR) domains via nicotinamide adenine dinucleotide (oxidized form) (NAD + ) hydrolysis. We show that v-cADPR (2′cADPR) v2-cADPR (3′cADPR) cyclized O-glycosidic bond formation between the ribose moieties in ADPR. Structures of 2′cADPR-producing TIR reveal conformational changes lead to an active assembly resembles those Toll-like adaptor domains....

10.1126/science.adc8969 article EN Science 2022-09-01

Lasso peptides are ribosomally synthesized and post-translationally modified (RiPPs) that possess a unique "lariat knot" structural motif. Genome mining-targeted discovery of new natural products from microbes obtained extreme environments has led to the identification gene cluster directing biosynthesis lasso peptide, designated as chaxapeptin 1, in genome Streptomyces leeuwenhoekii strain C58 isolated Atacama Desert. Subsequently, 1 was characterized using high-resolution electrospray...

10.1021/acs.joc.5b01878 article EN The Journal of Organic Chemistry 2015-09-24

Abstract An improved method for the synthesis of tethered ruthenium(II) complexes monosulfonylated diamines is described, together with their application to hydrogenation ketones and aldehydes. The were applied directly, in chloride form, asymmetric ketone hydrogenation, give products excess 99% ee best cases, using 30 bar hydrogen at 60 °C, selective reduction aldehydes over other functional groups.

10.1002/adsc.201200362 article EN Advanced Synthesis & Catalysis 2012-08-22

A ferrocene-based ditopic receptor containing a urea and benzocrown ether unit shows remarkable colour switching (ON-and-OFF) function induced by anion cation recognition.

10.1039/b210227g article EN Chemical Communications 2002-12-19

Half-sandwich Rh<sup>III</sup> anticancer complexes with activated Cp* rings not only undergo sequential CH<sub>3</sub> H–D exchange, but also react biological dienes, generating Rh<sup>I</sup> Diels–Alder adducts in aqueous media at ambient temperature.

10.1039/c7sc05058e article EN cc-by Chemical Science 2018-01-01

Silicon anodes require polymer binder systems that are both mechanically robust and electrochemically stable, to accommodate the dramatic volume expansion experienced during cycling operation. Herein, we report use of a poly(acrylic acid)-grafted styrene–butadiene rubber (PAA-g-SBR) with 80% partially neutralized Na-PAA as system for silicon-graphite anodes. The PAA-g-SBR graft copolymer was synthesized by grafting tert-butyl acrylate onto SBR treating intermediate H3PO4. PAA-g-SBR/Na-PAA...

10.1021/acsaem.2c03489 article EN cc-by ACS Applied Energy Materials 2022-12-22

Thermoresponsive polymers have attracted huge interest as a way of developing smart/adaptable materials for biomedicine, particularly due to changes in their solubility above the LCST. However, temperature is not always an appropriate or desirable stimulus given variety other cellular microenvironments that exist, including pH, redox potentials, ionic strength, and metal ion concentration. Here, we achieve highly specific, isothermal switch poly(N-isopropylacrylamide) by application ferric...

10.1021/mz500686w article EN ACS Macro Letters 2014-11-13

Mycobacterium tuberculosis ( Mtb ), the aetiological agent of tuberculosis, has evolved to scavenge nutrients from confined environment host macrophages with mycobacterial ATP-binding cassette (ABC) transporters playing a key role in nutrient acquisition. -UspC (Rv2318) is solute-binding protein essential transporter UspABC, one four ABC implicated by homology sugar Herein, we report structural and functional characterization -UspC. The 1.5 Å resolution structure UspC reveals two subdomain...

10.1098/rsob.160105 article EN cc-by Open Biology 2016-06-01

A new strategy for the asymmetric synthesis of chiral primary alpha-ferrocenylalkylamines has been utilized to generate homochiral redox-active receptors that bind carboxylate anions with moderate enantioselectivity and undergo a redox response complexation. [structure: see text]

10.1021/ol020162v article EN Organic Letters 2002-10-24

A method for probing the strength of B–N dative bonds is reported. The activation parameters nitrogen inversion in a series azetidines tethered to boronate esters have been quantified by VT-NMR and measured barriers correlated with data obtained 11B NMR, X-ray crystallography MP2 calculations.

10.1039/c3cc36159d article EN Chemical Communications 2013-01-01

Combination of four well-established techniques complemented with temperature dependence for probing structural changes and detecting differences between insulin samples.

10.1039/c6ay01573e article EN Analytical Methods 2016-01-01

A water-soluble fluorine magnetic resonance spectroscopy host-guest probe, P(HPA-co-AdamCF3A), was successfully constructed from the facile synthesis of a bifunctional monomer via quantitative Passerini reaction. Supramolecular complexation with (2-hydroxypropyl)-β-cyclodextrin promoted change in chemical environment, leading to modulation both relaxation properties as well shift moieties. This used probe supramolecular interaction by 19F MRI and give insight into formulation. work provides...

10.1021/acsmacrolett.9b00626 article EN ACS Macro Letters 2019-10-15

Sulfonyl ethylenediamine Ru( ii ) arene transfer hydrogenation catalysts can have high anticancer activity, but react rapidly with thiols, forming bridged dinuclear complexes.

10.1039/d1dt03856g article EN cc-by Dalton Transactions 2022-01-01

A series of 18-electron complexes general formula [Ru(p-cym)(1,2-dicarba-closo-dodecaborane-1,2-dithiolato)(L)] (p-cym = para-cymene; L 4-dimethylaminopyridine (2), nicotinamide (3), 3-ethynylpyridine (4), N-methylimidazole (5), 4-cyanopyridine (6), and pyridine (7)) were synthesised by reactions between the 16-electron precursor [Ru(p-cym)(1,2-dicarba-closo-dodecaborane-1,2-dithiolato)] (1) corresponding heterocyclic bases. X-ray crystal structures 2 5 determined. In dichloromethane...

10.1039/c2dt32650g article EN Dalton Transactions 2012-12-07

Abstract Dinuclear trihydroxido‐bridged osmium–arene complexes are inert and biologically inactive, but we show here that linking dihydroxido‐bridged Os II –arene fragments by a bridging di‐imine to form metallacycle framework results in strong antiproliferative activity towards cancer cells distinctive knotting of DNA. The shortened spacer length reduces biological stability solution decomposition inactive dimers. Significant differences behavior toward plasmid DNA condensation correlated...

10.1002/anie.201602995 article EN cc-by Angewandte Chemie International Edition 2016-05-30

Four verdazyl radicals, with varying substituents at the 3-position, were synthesised and used to prepare unimolecular initiators for use in stable free radical mediated living polymerisation of styrene n-butyl acrylate. The addition bulky differing electronic structures 3-position ring was investigated effects these on properties studied. nature substituent discovered affect rate characteristics polymerisation. acrylate homopolymers chain extended provide evidence as end group polymers.

10.1039/c2py20217d article EN Polymer Chemistry 2012-01-01

Interaction of the reactive 14 VE {Ir(IBioxMe4)3}(+) fragment with fluoroarenes results exclusively in ortho-C-H bond oxidative addition and formation 16 Ir(iii) derivatives [Ir(IBioxMe4)3(Ar)H](+) (Ar = 2-C6H4F, 2,3-C6H3F2, 2,4,6-C6H2F3). The C-H activation reactions occur under mild conditions are reversible.

10.1039/c5cc00529a article EN cc-by Chemical Communications 2015-01-01

New insights on the impact of hydrogen bonding and electrostatic interactions temperature-dependencies self-healing electromechanical properties dielectric elastomers.

10.1039/d0tc00509f article EN Journal of Materials Chemistry C 2020-01-01

A strong 11B {1H} nuclear Overhauser effect (NOE) enhancement can be observed in solid-state NMR spectra of borane adducts, yielding fractional enhancements, fI{S} = (I − I0)/I0, the magic angle spinning (MAS) signal up to 155%. This is an interesting and unusual observation as (spin I 3/2) a quadrupolar nucleus corresponding NOE completely absent solution. More generally, it shows that may have wider role play studies dynamics than has been envisaged hitherto.

10.1021/ja0610939 article EN Journal of the American Chemical Society 2006-05-01

The synthesis and characterization of five-coordinate rhodium(III) iridium(III) complexes the form [M(PNP-Np)(biph)][BArF4] are described, where PNP-Np is neopentyl-substituted pincer ligand 2,6-(Np2PCH2)2C5H3N (Np = CH2tBu), biph 2,2′-biphenyl, ArF 3,5-(CF3)2C6H3. These notable for adoption δ-agostic interactions in solid state, as evidenced by X-ray crystallography (50–150 K) ATR-IR spectroscopy, but structurally dynamic solution, exhibiting pseudorotation on 1H NMR time scale (185–308 K)....

10.1021/acs.organomet.4c00081 article EN cc-by Organometallics 2024-05-03

Lithiation and alkylation of a 2-isopropylidineaziridine bearing an (S)-alpha-methylbenzyl group on nitrogen proceeds with high levels diastereocontrol (80-90% de).

10.1039/b303252c article EN Chemical Communications 2003-01-01

Subnanometer-scale silicon dioxide (SiO2) films are frequently present before, during, and after device processing, yet they offer minimal surface passivation can detrimentally impact subsequent processing steps. Here we develop a process whereby the of nanometer subnanometer SiO2 is enhanced by up to 2 orders magnitude simple room temperature treatment using superacid bis(trifluoromethane)sulfonimide (TFSA, sometimes TFSI). By accurately modeling effective lifetime curves corresponding...

10.1021/acsaem.1c02935 article EN cc-by ACS Applied Energy Materials 2022-01-24
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