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Mostrando 841 - 860 Resultados de 1,845 Para Buscar 'fulereno~', tiempo de consulta: 3.35s Limitar resultados
  1. 841
    “…Correction for ‘ThC(2)@C(82)versus Th@C(84): unexpected formation of triangular thorium carbide cluster inside fullerenes’ by Yi Shen et al., Chem. Sci., 2022, https://doi.org/10.1039/d2sc04846a.…”
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    Correction: ThC(2)@C(82)versus Th@C(84): unexpected formation of triangular thorium carbide cluster inside fullerenes
  2. 842
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    Dibenzo[b,g]indeno­[1′,2′:3,4]fluoreno[1,2-d]oxonine-5,11,16,21-tetra­one
  3. 843
    “…The influence of a water-soluble [60] fullerene derivative containing five residues of 3-phenylpropionic acid and a chlorine addend appended to the carbon cage (F-828) on serum-starving human embryo lung diploid fibroblasts (HELFs) was studied. …”
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    Functionalized Fullerene Increases NF-κB Activity and Blocks Genotoxic Effect of Oxidative Stress in Serum-Starving Human Embryo Lung Diploid Fibroblasts
  4. 844
    “…The values of V (oc) of the organic solar cells for the SM1 acceptor (1.06 V and 1.02 V without and with solvent additive) are the highest values reported for devices based on non-fullerene acceptors to the best of our knowledge. The energy loss (E (loss)) of 0.56 eV and 0.48 eV for SM1 and SM2 based devices, respectively is one of the smallest reported for BHJ organic solar cells.…”
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    Donor–acceptor–acceptor (D–A–A) type 1,8-naphthalimides as non-fullerene small molecule acceptors for bulk heterojunction solar cells
  5. 845
    “…We report a high-resolution photoelectron imaging study of cryogenically-cooled H(2)O@C(60)(–) and H(2)O@C(59)N(–) endohedral fullerene anions. The electron affinity (EA) of H(2)O@C(60) is measured to be 2.6923 ± 0.0008 eV, which is 0.0088 eV higher than the EA of C(60), while the EA of H(2)O@C(59)N is measured to be 3.0058 eV ± 0.0007 eV, which is 0.0092 eV lower than the EA of C(59)N. …”
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    Probing the interaction between the encapsulated water molecule and the fullerene cages in H(2)O@C(60)(–) and H(2)O@C(59)N(–)
  6. 846
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    Designing an asymmetrical isomer to promote the LUMO energy level and molecular packing of a non-fullerene acceptor for polymer solar cells with 12.6% efficiency
  7. 847
    “…The results show the potential for the fabrication of efficient non-fullerene OSCs with low-temperature metal oxide selective layers.…”
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    Enhanced Performance of Inverted Non-Fullerene Organic Solar Cells by Using Metal Oxide Electron- and Hole-Selective Layers with Process Temperature ≤150 °C
  8. 848
    “…Ten novel fullerene-derivatives (FDs) of C(60) and C(70) had been designed as acceptor for polymer solar cell (PSC) by employing the quantitative structure-property relationship (QSPR) model, which was developed strategically with a reasonably big pool of experimental power conversion efficiency (PCE) data. …”
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    Optoelectronic Properties of C(60) and C(70) Fullerene Derivatives: Designing and Evaluating Novel Candidates for Efficient P3HT Polymer Solar Cells
  9. 849
    “…The incorporation of fullerene C(60) in the ECM/niche may be an alternative treatment for hepatocellular carcinoma.…”
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    Mechano-signalling, induced by fullerene C(60) nanofilms, arrests the cell cycle in the G2/M phase and decreases proliferation of liver cancer cells
  10. 850
    “…Lower water solubility levels limit the bio-applications of fullerene. Hence, to improve the water solubility of fullerene, while retaining its radical scavenger functions, a fullerene derivative, fullerenol C(60)(OH)(36), was synthesized, to examine its biofunctions in PM-exposed human keratinocyte (HaCaT) cells. …”
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    Water-Soluble Fullerenol C(60)(OH)(36) toward Effective Anti-Air Pollution Induced by Urban Particulate Matter in HaCaT Cell
  11. 851
    “…Supported by the photoconductive effect of the ZnO:HO‐PBI hybrid interlayers, improved electron collection and transportation is achieved in fullerene and non‐fullerene polymer solar cell devices, leading to remarkable power conversion efficiencies of up to 15.95 % for a non‐fullerene based organic solar cell.…”
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    Tetrahydroxy‐Perylene Bisimide Embedded in a Zinc Oxide Thin Film as an Electron‐Transporting Layer for High‐Performance Non‐Fullerene Organic Solar Cells
  12. 852
    “…Our results elucidate the general relevance of this degradation mechanism to both polymer:fullerene and polymer:nonfullerene blends and highlight the necessity of designing electron acceptor materials with sufficient electron affinities to overcome this challenge, thereby paving the way toward achieving long-term solar cell stability with minimal device encapsulation.…”
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    Toward Improved Environmental Stability of Polymer:Fullerene and Polymer:Nonfullerene Organic Solar Cells: A Common Energetic Origin of Light- and Oxygen-Induced Degradation
  13. 853
    por Liu, Yan-Zhi, Zhang, Jian-Bin, Yuan, Kun
    Publicado 2020
    “…In addition, the frontier molecular orbital (FMO) features and intermolecular weak interaction region between DSCPP and fullerenes gusts are discussed to further understand the structures and properties of the DSCPP⊃fullerene systems. …”
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    Theoretical Prediction on a Novel Reduction-Responsive Nanoring Having a Disulfide Group for Facile Encapsulation and Release of Fullerenes C(60) and C(70)
  14. 854
    “…A study was carried out on the possibility of orderly and spontaneous dimerization at room temperature of C(60) cages in fullerene liquid crystal fullerene dyads (R-C(60)). …”
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    Exohedral Functionalization of Fullerene by Substituents Controlling of Molecular Organization for Spontaneous C(60) Dimerization in Liquid Crystal Solutions and in a Bulk Controlled by a Potential
  15. 855
    “…The current study suggested that carbon fullerene and nanotube demonstrated significant binding towards the prioritized multi-targets of SARS-CoV-2. …”
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    Carbon fullerene and nanotube are probable binders to multiple targets of SARS-CoV-2: Insights from computational modeling and molecular dynamic simulation studies
  16. 856
    “…The sensitivity of pure and doped X(12)N(12) (X = B and Al) fullerene-like nano-cages (FLNs) toward the anti-cancer drug temozolomide (TMZ) is probed herein at DFT/M06-2X-D3/6-311G(d,p) theoretical level in both gas phase and water. …”
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    DFT investigation on the application of pure and doped X(12)N(12) (X = B and Al) fullerene-like nano-cages toward the adsorption of temozolomide
  17. 857
    “…Generally, cyclopropanated fullerene derivatives are obtained by the standard Bingel–Hirsch procedure. …”
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    Selective formation of dihydrofuran fused [60] fullerene derivatives by TEMPO mediated [3 + 2] cycloaddition of medium chain β-keto esters to C(60)
  18. 858
    “…Stable and highly conductive self-n-doped fullerene ammonium halides are promising optoelectronic materials. …”
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    Self-assembly of highly conductive self-n-doped fullerene ammonium halides and their application in the in situ solution-processable fabrication of working electrodes for alcohol electrooxidation
  19. 859
    “…Therefore, the nanosized carbon molecule, C(60) fullerene, as a powerful antioxidant, is very attractive. …”
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    Analysis of Biomechanical and Biochemical Markers of Rat Muscle Soleus Fatigue Processes Development during Long-Term Use of C(60) Fullerene and N-Acetylcysteine
  20. 860
    “…We designed and synthesized an asymmetric non-fullerene small molecule acceptor (NF-SMA) IDT-TNIC with an A–D–π–A structure, based on an indacenodithiophene (IDT) central core, with a unidirectional non-fused alkylthio-thiophene (T) π-bridge, and 2-(3-oxo-2,3-dihydro-1H-cyclopenta[b]naphthalen-1-ylidene)malononitrile (NIC) extended terminal groups. …”
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    Asymmetric Non-Fullerene Small Molecule Acceptor with Unidirectional Non-Fused π-Bridge and Extended Terminal Group for High-Efficiency Organic Solar Cells
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