ISSN:
eISSN:
Dyscypliny:
- inżynieria chemiczna (Dziedzina nauk inżynieryjno-technicznych)
- biologia medyczna (Dziedzina nauk medycznych i nauk o zdrowiu)
- nauki farmaceutyczne (Dziedzina nauk medycznych i nauk o zdrowiu)
- nauki biologiczne (Dziedzina nauk ścisłych i przyrodniczych)
- nauki chemiczne (Dziedzina nauk ścisłych i przyrodniczych)
Punkty Ministerialne: Pomoc
Rok | Punkty | Lista |
---|---|---|
Rok 2024 | 200 | Ministerialna lista czasopism punktowanych 2024 |
Rok | Punkty | Lista |
---|---|---|
2024 | 200 | Ministerialna lista czasopism punktowanych 2024 |
2023 | 200 | Lista ministerialna czasopism punktowanych 2023 |
2022 | 200 | Lista ministerialna czasopism punktowanych (2019-2022) |
2021 | 200 | Lista ministerialna czasopism punktowanych (2019-2022) |
2020 | 200 | Lista ministerialna czasopism punktowanych (2019-2022) |
2019 | 200 | Lista ministerialna czasopism punktowanych (2019-2022) |
2018 | 45 | A |
2017 | 45 | A |
2016 | 45 | A |
2015 | 45 | A |
2014 | 45 | A |
2013 | 45 | A |
2012 | 45 | A |
2011 | 45 | A |
2010 | 40 | A |
Model czasopisma:
Punkty CiteScore:
Rok | Punkty |
---|---|
Rok 2023 | 26.6 |
Rok | Punkty |
---|---|
2023 | 26.6 |
2022 | 26.3 |
2021 | 23.9 |
2020 | 21.7 |
2019 | 20.8 |
2018 | 20.2 |
2017 | 19.7 |
2016 | 18.7 |
2015 | 19 |
2014 | 18.3 |
2013 | 17 |
2012 | 16.5 |
2011 | 16.7 |
Impact Factor:
Sherpa Romeo:
Prace opublikowane w tym czasopiśmie
Filtry
wszystkich: 14
Katalog Czasopism
Rok 2024
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Pendant Proton-Relays Systematically Tune the Rate and Selectivity of Electrocatalytic Ammonia Generation in a Fe-Porphyrin Based Metal-Organic Framework
PublikacjaElectrocatalytic nitrite reduction (eNO2RR) is a promising alternative route to produce ammonia (NH3). Until now, several molecular catalysts have shown capability to homogeneously reduce nitrite to NH3, while taking advantage of added secondary-sphere functionalities to direct catalytic performance. Yet, realizing such control over heterogeneous electrocatalytic surfaces remains a challenge. Herein, we demonstrate that heterogenization...
Rok 2022
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Ln2(SeO3)2(SO4)(H2O)2 (Ln=Sm, Dy, Yb): A Mixed‐Ligand Pathway to New Lanthanide(III) Multifunctional Materials Featuring Nonlinear Optical and Magnetic Anisotropy Properties
PublikacjaBottom-up assembly of optically nonlinear and magnetically anisotropic lanthanide materials involving precisely placed spin carriers and optimized metal-ligand coordination offers a potential route to developing electronic architectures for coherent radiation generation and spin-based technologies, but the chemical design historically has been extremely hard to achieve. To address this, we developed a worthwhile avenue for creating...
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Topochemical, Single‐Crystal‐to‐Single‐Crystal [2+2] Photocycloadditions Driven by Chalcogen‐Bonding Interactions
PublikacjaThe face-to-face association of (E)-1,2-di(4-pyridyl)ethylene (bpen) molecules into rectangular motifs stabilized for the first time by chalcogen bonding (ChB) interactions is shown to provide photoreactive systems leading to cyclobutane formation through single-crystal-to-single-crystal [2+2] photodimerizations. The chelating chalcogen bond donors are based on original aromatic, ortho-substituted bis(selenocyanato)benzene derivatives...
Rok 2021
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Enantioselective Gel Phase Synthesis of Metal–Organic Materials
Publikacja -
Folding‐upon‐repair DNA nanoswitches for monitoring DNA repair enzymes activity
PublikacjaWe demonstrate here a new class of DNA‐based nanoswitches that, upon enzymatic repair, could undergo a conformational change mechanism leading to a change in fluorescent signal. Such folding‐upon‐repair DNA nanoswitches are synthetic DNA sequences containing O6‐methyl‐guanine (O6‐MeG) nucleobases and labelled with a fluorophore/quencher optical pair. The nanoswitches are rationally designed so that only upon enzymatic demethylation...
Rok 2020
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Developing Luminescent Ratiometric Thermometers Based on a Covalent Organic Framework (COF)
Publikacja
Rok 2018
Rok 2016
Rok 2015
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Optimization of Hydrogen - Evolving Photochemical Molecular Devices
PublikacjaA molecular photocatalyst consisting of a RuII photocenter, a tetrapyridophenazine bridging ligand, and a PtX2 (X=Cl or I) moiety as the catalytic center functions as a stable system for light-driven hydrogen production. The catalytic activity of this photochemical molecular device (PMD) is significantly enhanced by exchanging the terminal chlorides at the Pt center for iodide ligands. Ultrafast transient absorption spectroscopy...
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Palladium versus Platinum: The Metal in the Catalytic Center of a Molecular Photocatalyst Determines the Mechanism of the Hydrogen Production with Visible Light
PublikacjaTo develop highly efficient molecular photocatalysts for visible light-driven hydrogen production, a thorough understanding of the photophysical and chemical processes in the photocatalyst is of vital importance. In this context, in situ X-ray absorption spectroscopic (XAS) investigations show that the nature of the catalytically active metal center in a (N^N)MCl2 (M=Pd or Pt) coordination sphere has a significant impact on the...
Rok 2012
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Hunting for the Magnesium(I) Species: Formation, Structure, andReactivity of some Donor-Free Grignard Compounds
PublikacjaMagnesium bromide radicals have to be prepared as high-temperature molecules and trapped as a metastable solution because a seemingly simple reduction of donor-free Grignard compounds failed. However, the essential role of magnesium(I) species during the formation of Grignard compounds could be demonstrated experimentally.
Rok 2005
Rok 2003
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Supramolecular Assemblies of Hydrogen Bonded Carboxylic Acid Dimers Mediated by Phenyl-Pentafluorophenyl Stacking Interactions.
PublikacjaKwas pentafluorobenzoesowy tworzy heterodimery z kwasami benzoesowym i 2,4,6-trimetylobenzoesowym w wyniku oddziaływań typu pi-pi reszt fenylowych i pentafluorofenylowych. Otrzymane kokryształy wymienionych kwasów z 1,4-bisarylobutadiynami zawierały homodimery tworzone przez cząsteczki kwasów, pomiędzy którymi znajdowały się cząsteczki diarylodiacetylenów.
Rok 2002
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Enantiomeric self-recognition of a facial amphiphile triggered by [{Pd(ONO2)(en)}2]
PublikacjaOpisano syntezę pochodnych glikolurylu tworzących dimeryczne struktury w roztworze wodnym prowadzące do samorozpoznania enancjomerycznego. Struktury te uzyskano dzięki koordynacji do [{Pd(ONO2)(en)}2].
wyświetlono 1658 razy