Calixarene Complexes: Synthesis, Properties and Applications |
Autore | Berberan-Santos Mario |
Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
Descrizione fisica | 1 electronic resource (198 p.) |
Soggetto topico | Research & information: general |
Soggetto non controllato |
thiosemicarbazone
calix[4]arene metal complex X-ray structure antimicrobial anticancer copper supramolecular inclusion complex fluorescence sensor density functional theory calix[3]arenes metacyclophanes calixarene-analogous metacyclophanes inherent chirality host-guest chemistry dihomooxacalix[4]arenes naphthyl(thio)urea anion receptors alkylammonium hydrochlorides ditopic receptors chiral recognition NMR studies UV-Vis absorption studies fluorescence studies X-ray diffraction DFT calculations calixarene resorcinarene pillararene antibiotic fungicide biofilm inhibition calixarenes threading chirality barfate salts pseudorotaxane chiral axles chiral wheels calixarene-like structure polyoxometalates nitronate crystal structure host–guest chemistry anion receptor anion sensors lanthanides UV–vis studies quantum yields lifetime measurements noncovalent synthesis hierarchical control calix[4]tubes metallo-porphyrins phthalimide derivatives conventional synthesis microwave irradiation ball milling NMR spectroscopy electronic absorption and fluorescence studies |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Altri titoli varianti | Calixarene Complexes |
Record Nr. | UNINA-9910557365803321 |
Berberan-Santos Mario
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Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
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Lo trovi qui: Univ. Federico II | ||
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Nitro Compounds and Their Derivatives in Organic Synthesis |
Autore | Nishiwaki Nagatoshi |
Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
Descrizione fisica | 1 electronic resource (120 p.) |
Soggetto topico | Research & information: general |
Soggetto non controllato |
nitro
pyridone 1-methyl-2-quinolone cycloaddition direct functionalization perylenediimide nitro group organic materials Phenacylation of beta-nitropyridin-2-ones 8-nitro-5-RO-indolizines oxazole-pyrrole ring transformation conjugate addition dihydrofuran 1,3-dicarbonyl compound enolate isoxazoline N-oxide nitroketone nitronate nucleophilic substitution nitropyridines isoxazolo[4,3-b]pyridines 1,4-dihydropyridines nucleophilic addition Diels-Alder reaction dearomatization hexapyrrolohexaazacoronene nitration SNAr substitution ICT character aromaticity C–H functionalization total synthesis pyrrolidines anchimeric assistance epimerization PDE4 inhibitors 1,3-Dipole electron-withdrawing ability electrophilicity nucleophilicity |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910557494003321 |
Nishiwaki Nagatoshi
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Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
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Lo trovi qui: Univ. Federico II | ||
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