Intramolecular Hydrogen Bonding 2021
| Intramolecular Hydrogen Bonding 2021 |
| Autore | Jabłoński Mirosław |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (246 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
AIM
amino-alcohols beryllium bonds bond energy estimation calculated infrared spectra CCSD charge-transfer interactions CPMD crystalline phase deuterium isotope effects on chemical shifts DFT DSC excited-state intramolecular proton transfer fragmentation methods FT-IR gas phase high-accuracy extrapolation methods Hirshfeld surface analysis hydrogen bond hydrogen bond (HB) hydrogen bond energies IINS inelastic incoherent neutron scattering interacting quantum atoms interaction energy intramolecular hydrogen bond (IHB) intramolecular hydrogen bonding intramolecular hydrogen bonds intramolecular interaction isomerization isotope ratios isotopic effect local vibrational modes matrix isolation molecular dynamics molecular tailoring approach (MTA) MP2 N-salicylidene aniline derivative n/a nitro group non-covalent interactions noncovalent interactions NQR nuclear quantum effects phase transition photobiology photochemistry photophysical properties polymorphism QTAIM quantum chemistry Raman resonance-assisted hydrogen bond SAPT Schiff base Schiff bases solvatochromism spin-spin coupling constants structures and binding energies ultrafast processes X-ray α-substitution |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557663903321 |
Jabłoński Mirosław
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Lo trovi qui: Univ. Federico II | ||
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Nitro Compounds and Their Derivatives in Organic Synthesis
| 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 online resource (120 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
1-methyl-2-quinolone
1,3-dicarbonyl compound 1,3-Dipole 1,4-dihydropyridines 8-nitro-5-RO-indolizines anchimeric assistance aromaticity C-H functionalization conjugate addition cycloaddition dearomatization Diels-Alder reaction dihydrofuran direct functionalization electron-withdrawing ability electrophilicity enolate epimerization hexapyrrolohexaazacoronene ICT character isoxazoline N-oxide isoxazolo[4,3-b]pyridines nitration nitro nitro group nitroketone nitronate nitropyridines nucleophilic addition nucleophilic substitution nucleophilicity organic materials oxazole-pyrrole ring transformation PDE4 inhibitors perylenediimide Phenacylation of beta-nitropyridin-2-ones pyridone pyrrolidines SNAr substitution total synthesis |
| 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 | ||
| Lo trovi qui: Univ. Federico II | ||
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