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Intramolecular N−H...O hydrogen bonding, quinoid effect, and partial π-electron delocalization in N-aryl Schiff bases of 2-hydroxy-1-naphthaldehyde: the crystal structures of planar N-(α-naphthyl)- and N-(β-naphthyl)-2-oxy-1-naphthaldimine
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Structure of thermochromic Schiff bases. II. Structures of N-salicylidene-3-aminopyridine and N-(5-methoxysalicylidene)-3-aminopyridine
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inferred← citeshttps://doi.org/10.1081/sl-100107900openalex-snapshot
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inferred← citeshttps://doi.org/10.1081/sl-120039588openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270100007290openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270100015535openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270101000993openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270104022565openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270107005689openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s0108270109006696openalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s1600536802003057openalex-snapshot
N-(3-Chlorophenyl)-2-hydroxy-1-naphthaldimine at 200 K
inferred← citeshttps://doi.org/10.1107/s1600536803029222openalex-snapshot
1-[N-(p-Hydroxyphenyl)aminomethylidene]naphthalen-2(1H)-one propan-1-ol hemisolvate
inferred← citeshttps://doi.org/10.1107/s1600536804002971openalex-snapshot
1-[(3-Hydroxypyridin-2-ylamino)methylene]naphthalen-2(1H)-one
inferred← citeshttps://doi.org/10.1107/s1600536804008827openalex-snapshot
1-[(2-Hydroxy-5-methylphenylamino)methylene]naphthalen-2(1H)-one
inferred← citeshttps://doi.org/10.1107/s1600536804008864openalex-snapshot
1-[(4-Nitrophenylamino)methylene]naphthalen-2(1H)-one
inferred← citeshttps://doi.org/10.1107/s1600536804013728openalex-snapshot
1-[(5-Chloro-2-hydroxyphenylamino)methylene]naphthalen-2(1H)-one
inferred← citeshttps://doi.org/10.1107/s160053680603131xopenalex-snapshot
trans-Tetrachlorobis{1-[(2,6-diisopropylphenyl)iminiomethyl]-2-naphtholato-κO}zirconium(IV) dichloromethane disolvate
inferred← citeshttps://doi.org/10.1107/s1600536811040918openalex-snapshot
1,1′-[m-Phenylenebis(nitrilomethanylylidene)]dinaphthalen-2-ol–1,1′-[m-phenylenebis(iminomethanylylidene)]dinaphthalen-2(1H)-one (0.58/0.42)
inferred← citeshttps://doi.org/10.1107/s1600536811041870openalex-snapshot
1-[(4-{[(2-Oxo-1,2-dihydronaphthalen-1-ylidene)methyl]amino}anilino)methylidene]naphthalen-2(1H)-one dihydrate
inferred← citeshttps://doi.org/10.1107/s1600536813016474openalex-snapshot
Ethyl 2-[(2-hydroxybenzylidene)amino]-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate
inferred← citeshttps://doi.org/10.1139/v04-021openalex-snapshot
Electrochemical behaviour of 1-{[(3-halophenyl)imino]methyl}-2-naphthol Schiff bases on graphite electrodes
inferred← citeshttps://doi.org/10.14233/ajchem.2018.21286openalex-snapshot
Schiff Bases Derived from 2-Hydroxynaphthalene-1-carbaldehyde and their Metal Complexes
inferred← citeshttps://doi.org/10.1524/zkri.2006.221.10.699openalex-snapshot
A crystallographic and spectroscopic study on the imine-amine tautomerism of 2-hydroxyaldimine compounds
inferred← citeshttps://doi.org/10.1524/zkri.220.7.639.67102openalex-snapshot
Synthesis, crystal structure and electrochemical behaviour of water soluble Schiff bases
inferred← citeshttps://doi.org/10.20450/mjcce.2010.159openalex-snapshot
Schiff bases derived from hydroxyaryl aldehydes: molecular and crystal structure, tautomerism, quinoid effect, coordination compounds
inferred← citeshttps://doi.org/10.2116/analsci.16.553openalex-snapshot
Crystal Structure of 1,5-Di[N-2-oxyphenyl-salicylidene]-3-oxapentane
inferred← citeshttps://doi.org/10.2116/analsci.16.99openalex-snapshot
Crystal Structure of 1-[N -(6-Methyl-2-pyridyl)aminomethylidene] 2(1 H)-naphthalenone
inferred← citeshttps://doi.org/10.2116/analsci.17.1021openalex-snapshot
Crystal Structure of 1-[N-(4-Fluorophenyl)]naphthaldimine
inferred← citeshttps://doi.org/10.2116/analsci.17.679openalex-snapshot
Crystal Structure of N,N-Bis(4-hydroxy-benzylidine)ethylenediamine•methanol
inferred← citeshttps://doi.org/10.2116/analsci.18.1281openalex-snapshot
Crystal Structure of 4-{[(1E)-(3,5-dinitro-2-hydroxyphenyl)-methylidene]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one·acetonitrile
inferred← citeshttps://doi.org/10.2116/analsci.18.215openalex-snapshot
Crystal Structure of 4-{[(1E)-(2-Hydroxynaphthyl)methylidene]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one
inferred← citeshttps://doi.org/10.2116/analscix.22.x115openalex-snapshot
Crystal Structure of 2-Hydroxynaphthaldehyde[(1E)-(2-hydroxynaphthyl)methylene]hydrazone
inferred← citeshttps://doi.org/10.3390/12081796openalex-snapshot
Synthesis of Some New Anils: Part 1. Reaction of 2-Hydroxy-benzaldehyde and 2-Hydroxynaphthaldehyde with 2-Aminopyridene and 2-Aminopyrazine
inferred← citeshttps://doi.org/10.3390/antibiotics12111634openalex-snapshot
Antimicrobial Activity of Novel Ni(II) and Zn(II) Complexes with (E)-2-((5-Bromothiazol-2-yl)imino)methyl)phenol Ligand: Synthesis, Characterization and Molecular Docking Studies
inferred← citeshttps://doi.org/10.3390/inorganics10040043openalex-snapshot
Transition Metal Complexes of Schiff Base Ligands Prepared from Reaction of Aminobenzothiazole with Benzaldehydes
inferred← citeshttps://doi.org/10.4137/oci.s3687openalex-snapshot
Spectroscopic Study and Semi-empirical Calculations of Tautomeric Forms of Schiff Bases Derived from 2-hydroxy- 1-naphthaldehyde and Substituted 2-aminothiophene
inferred← citeshttps://doi.org/10.5562/cca2111openalex-snapshot
Controlling Solvate Formation of a Schiff Base by Combining Mechano-chemistry with Solution Synthesis
inferred← citeshttps://doi.org/10.5562/cca3907openalex-snapshot
Transition Metal-Mediated Hydrolysis of the Imine Bond in 2-Azomethine Benzothiazoles
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