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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  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui