Mostrando 3,101 - 3,120 Resultados de 10,256 Para Buscar '"donating"', tiempo de consulta: 0.42s Limitar resultados
  1. 3101
    “…After reaction with H(2)S, the strong electron-withdrawing group dinitrophenyl ether (which acts as both the recognition moiety and the fluorescence quencher) was cleaved and replaced by an electron-donating group hydroxyl. This correspondingly leads to the changes of the probe's electronic state and absorption red-shifting as well as the subsequent turn-on fluorescent and optoacoustic signals. …”
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  2. 3102
    “…When both aromatic rings have electron-donating di-methylamino substituents, the interaction is repulsive (+2.0 kJ mol(–1)) due to increased π-electron repulsion. …”
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  3. 3103
    “…Due to electron-withdrawing properties of purine and 7-deazapurine heterocycles, which were additionally extended by triazole moieties, the compounds with electron-donating groups showed intramolecular charge transfer character (ICT/TICT) of the excited states which was proved by solvatochromic dynamics and supported by DFT calculations. …”
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  4. 3104
    “…Oxidation of electron-donating thioalkyl substituents to electron-withdrawing sulfoxides or sulfones is a particularly effective modification. …”
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  5. 3105
    “…Our results reveal that when the proton donors D (which are electron-donating) and the proton acceptors A (which are electron-withdrawing) are grouped together as in DDAA, there is a larger accumulation of charge around the frontier atoms than when the proton donor and acceptor groups are alternating as in DADA. …”
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  6. 3106
    “…The substitution of both aniline groups, by either methoxy (electron donating effect) or fluorine (electron withdrawal effect), decreased the cytotoxicity in the aminoquinones. …”
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  7. 3107
    “…We show that the electron-donating effect of donor groups can enhance ligand-centered transitions and thoroughly eliminate cluster-centered excited states by delocalizing the molecular transition orbitals from the cluster unit to the ligand, leading to 13-fold increased photoluminescence quantum yield. …”
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  8. 3108
    “…The structure–emission relationship was further investigated by tailoring the electron‐donating functions to the anthracene moiety to give dyes 4 c–6 c with charge‐transfer character. …”
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  9. 3109
    “…The structure–property correlation of the fluoranthene-based HTMs was carefully investigated by tuning their structural geometry (linear vs. branched), connection between electron-donating and electron-withdrawing moieties (single bond vs. ethylene), and the substitution position of the methoxy side-groups (para- vs. meta-). …”
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  10. 3110
    “…Moreover, the neighboring Al (Al(III)) on the (111)(n) surface provides suitable acceptance position for the electron donating groups. The defected surfaces of (111)(n) are found to be having a similar stability. …”
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  11. 3111
    “…Similar to the PVK–C(60) and C(60) cages in general, the PVK–CDots exhibited significant photoinduced electron accepting characteristics and, at the same time, also extraordinary electron donating abilities that are not available to fullerenes. …”
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  12. 3112
    “…Herein, we report the luminescent behavior of three simple cyanostilbenes with triphenylamine-donating groups bearing different electron-withdrawing groups (phenyl, pyridyl, and p-nitrophenyl) in a common donor (D)−π–acceptor (A) α-cyanostilbene construct along with their thermal and electrochemical properties. …”
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  13. 3113
    “…[Image: see text] Croconaine dyes are appealing molecules synthesized via the condensation of croconic acid and reactive electron-donating aromatic or heterocyclic systems. Here, matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) investigation of indolenine-based croconaines is presented for the first time. …”
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  14. 3114
    “…[Image: see text] A new acceptor unit, fluorinated thieno[2′,3′:4,5]benzo[1,2-d][1,2,3]triazole (fBTAZT), has been designed and synthesized to build two donor–acceptor (D–A) copolymers with the none/fluorinated benzodithiophene (BDT) unit, which have been applied as the electron-donating material with ITIC as an electron-accepting material to fabricate the nonfullerene polymer solar cells (PSCs). …”
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  15. 3115
    “…In this work, we theoretically designed a ratiometric and NIR fluorescent sensor based on the 10-hydroxybenzo[h]quinoline (HBQ) backbone via systematically investigating the substituent effects of electron-donating groups (−NH(2), −CH(3), −C(CH(3))(3)) and electron-withdrawing groups (−NO(2), −CN, −F, −Cl, −CF(3)) at the proton donor site on the proton transfer process in HBQ in both the S(0) and the S(1) states. …”
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  16. 3116
    “…Electron-withdrawing groups (EWGs) and aromatic substituents in the exocyclic carbons tend to stabilize the OSS and T states, whereas electron-donating groups slightly destabilize them. For CS, OSS, and T states, aromaticity measures indicate a gain of aromaticity of the 6-membered rings of the CPHs with the increase in their size and when CPHs incorporate EWGs or aromatic substituents. …”
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  17. 3117
    “…The theoretical calculations showed that hyper-conjugation, the main underlying factor hindering the aerobic oxidation of tetrahydroisoquinolines, is relieved both by π- and σ-donating substituents. This mechanistic insight provided a novel photocatalytic route based on N-substituted auxiliaries that facilitated the conversion of tetrahydroisoquinolines into the corresponding isoquinolines in just three simple steps (yield 71.7% in bulk-solution phase), using unmodified Ru(bpy)(3)Cl(2) photocatalyst, sun energy, atmospheric O(2), and at ambient temperature.…”
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  18. 3118
    “…In-situ turbidity scanning and dynamic light scattering revealed distinct reaction kinetics for nPM and 3F, attributable to the electron withdrawing and donating nature of the fluoro- and organo-side chains of 3F and nPM, respectively.…”
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  19. 3119
    “…The 1-ethylpropyl group as rather short and branched alkyl substituent at the imide nitrogen and the n-propyl group as short and unbranched one at the core amines yielded the best solubilities. The electron-donating diaminoalkyl substituents together with the electron-deficient aromatic core of the naphthalene diimides increase the charge-transfer character of their photoexcited states and thus shift their absorption into the visible light (500–650 nm). …”
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  20. 3120
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