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Strongly Blue-Shifted C−H Stretches: Interaction of Formaldehyde with Hydrogen Fluoride Clusters
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-461x(2000)77:1<187::aid-qua17>3.0.co;2-3openalex-snapshot
Base properties of H2CO in the excited3n??* state
inferredcites →https://doi.org/10.1002/jcc.540040303openalex-snapshot
Efficient diffuse function‐augmented basis sets for anion calculations. III. The 3‐21+G basis set for first‐row elements, Li–F
inferredcites →https://doi.org/10.1002/jcc.540040419openalex-snapshot
MNDO calculations of proton and methyl‐and ethyl‐cation affinities of neutral carbon, nitrogen, and oxygen bases
inferredcites →https://doi.org/10.1002/jcc.540050304openalex-snapshot
Evaluation of MNDO calculated proton affinities
inferredcites →https://doi.org/10.1002/jcc.540060406openalex-snapshot
Basis set and correlation effects on computed proton affinities of some oxygen and nitrogen bases
inferredcites →https://doi.org/10.1002/poc.685openalex-snapshot
Hydrogen bonding strength—measures based on geometric and topological parameters
inferredcites →https://doi.org/10.1002/qua.20481openalex-snapshot
Long‐range π‐type hydrogen bond in dimers CH2HF, CH2OH2O, and CH2ONH3
inferredcites →https://doi.org/10.1002/qua.560430606openalex-snapshot
Proton affinities of molecules containing nitrogen and oxygen: comparing ab initio and semiempirical results to experiments
inferredcites →https://doi.org/10.1006/jmsp.1996.7229openalex-snapshot
Millimeter-Wave Spectra of H213COH+and D2COD+
inferredcites →https://doi.org/10.1007/978-1-349-02172-7openalex-snapshot
Hydrogen Bonding by C—H Groups
inferredcites →https://doi.org/10.1007/s007060200008openalex-snapshot
Hydrogen Bonding Properties of the Complexes of Formaldehyde and its Derivatives with HF and HCl
inferredcites →https://doi.org/10.1016/0009-2614(89)80049-1openalex-snapshot
On the angular shape of van der Waals dimers of small polar molecules
inferredcites →https://doi.org/10.1016/0009-2614(94)01273-3openalex-snapshot
An evaluation of the performance of density functional theory, MP2, MP4, F4, G2(MP2) and G2 procedures in predicting gas-phase proton affinities
inferredcites →https://doi.org/10.1016/0022-2852(87)90269-4openalex-snapshot
Rotational, structural, ab initio, and semirigid bender analysis of the millimeter wave spectrum of H2COHF
inferredcites →https://doi.org/10.1016/0301-0104(88)80023-5openalex-snapshot
Structure, energetics and vibrational spectra of H-bonded systems. Dimers and trimers of HF and HCl
inferredcites →https://doi.org/10.1016/j.molstruc.2004.02.040openalex-snapshot
Blue-shifting hydrogen bonds—are they improper or proper?
inferredcites →https://doi.org/10.1016/j.theochem.2004.09.006openalex-snapshot
The interaction of fluorosilanes with hydrogen fluoride clusters: strongly blue-shifted hydrogen bonds
inferredcites →https://doi.org/10.1016/s0009-2614(03)00770-xopenalex-snapshot
Valence and Rydberg states of protonated formaldehyde
inferredcites →https://doi.org/10.1016/s0301-0104(00)00079-3openalex-snapshot
Density functional calculations on simple carbonyl bases: protonation and hydrogen bond formation with water
inferredcites →https://doi.org/10.1016/s0301-0104(99)00045-2openalex-snapshot
Effect of protonation on the atomic and bond properties of the carbonyl group in aldehydes and ketones
inferredcites →https://doi.org/10.1016/s1386-1425(97)00247-3openalex-snapshot
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inferredcites →https://doi.org/10.1021/ar990008hopenalex-snapshot
The Interaction of Carbonyl Groups with Substituents
inferredcites →https://doi.org/10.1021/ja00057a009openalex-snapshot
Chemistry in superacids. 10. Role of oxonium, sulfonium, and carboxonium dications in superacid-catalyzed reactions
inferredcites →https://doi.org/10.1021/ja00064a058openalex-snapshot
Assigning absolute values to proton affinities: a differentiation between competing scales
inferredcites →https://doi.org/10.1021/ja00254a006openalex-snapshot
Barriers to rotation adjacent to double bonds. 3. The carbon-oxygen barrier in formic acid, methyl formate, acetic acid, and methyl acetate. The origin of ester and amide resonance
inferredcites →https://doi.org/10.1021/ja00285a033openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00316a034openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00374a017openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja00895a002openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja952871sopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jo00101a050openalex-snapshot
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inferredcites →https://doi.org/10.1021/jp001283kopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jp001672eopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jp0043470openalex-snapshot
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inferredcites →https://doi.org/10.1021/jp0131267openalex-snapshot
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inferredcites →https://doi.org/10.1021/jp020438gopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jp036048ropenalex-snapshot
Blue-Shifted Hydrogen-Bonded Complexes CF 3 H−(HF) 1 ≤ n ≤ 3
inferredcites →https://doi.org/10.1021/jp9710852openalex-snapshot
Ab Initio Molecular-Orbital Study of Hydrogen-Bonded Complexes of Carbonyl Aliphatic Compounds and Hydrogen Fluoride
inferredcites →https://doi.org/10.1021/jp981093yopenalex-snapshot
Base Properties of H2CO in the Excited 1n→π* State
inferredcites →https://doi.org/10.1021/jp984313gopenalex-snapshot
Molecular Electrostatic Potential as Reactivity Index in Hydrogen Bonding: Ab Initio Molecular Orbital Study of Complexes of Nitrile and Carbonyl Compounds with Hydrogen Fluoride
inferredcites →https://doi.org/10.1021/jp984541aopenalex-snapshot
Molecular Electrostatics for Exploring Complexes of Carbonyl Compounds and Hydrogen Fluoride
inferredcites →https://doi.org/10.1039/p29940000799openalex-snapshot
Theoretical studies of protonation and lithiation of first- and second-row aldehydes
inferredcites →https://doi.org/10.1063/1.1571517openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.1676210openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.430630openalex-snapshot
Molecular orbital theory of the hydrogen bond. X. Monosubstituted carbonyls as proton acceptors
inferredcites →https://doi.org/10.1063/1.438955openalex-snapshot
Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions
inferredcites →https://doi.org/10.1063/1.438980openalex-snapshot
Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11–18
inferredcites →https://doi.org/10.1063/1.444267openalex-snapshot
Self-consistent molecular orbital methods. XXIII. A polarization-type basis set for second-row elements
inferredcites →https://doi.org/10.1063/1.445174openalex-snapshot
The rotational and hyperfine spectrum and structure of H2CO–HF2
inferredcites →https://doi.org/10.1063/1.447079openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.462569openalex-snapshot
Electron affinities of the first-row atoms revisited. Systematic basis sets and wave functions
inferredcites →https://doi.org/10.1063/1.464303openalex-snapshot
Gaussian basis sets for use in correlated molecular calculations. III. The atoms aluminum through argon
inferredcites →https://doi.org/10.1063/1.466317openalex-snapshot
Carbonyl–water hydrogen bonding: The H2CO–H2O prototype
inferredcites →https://doi.org/10.1063/1.471531openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.472309openalex-snapshot
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inferredcites →https://doi.org/10.1063/1.555719openalex-snapshot
Evaluated Gas Phase Basicities and Proton Affinities of Molecules; Heats of Formation of Protonated Molecules
inferredcites →https://doi.org/10.1063/1.556018openalex-snapshot
Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update
inferredcites →https://doi.org/10.1080/00268977000101561openalex-snapshot
The calculation of small molecular interactions by the differences of separate total energies. Some procedures with reduced errors
inferredcites →https://doi.org/10.1080/00268979809482299openalex-snapshot
Explicitly correlated coupled cluster calculations of the dissociation energies and barriers to concerted hydrogen exchange of (HF)n oligomers (n = 2,3,4,5)
inferredcites →https://doi.org/10.1093/acprof:oso/9780198509707.001.0001openalex-snapshot
The Weak Hydrogen Bond
inferredcites →https://doi.org/10.1103/physrev.46.618openalex-snapshot
Note on an Approximation Treatment for Many-Electron Systems
inferredcites →https://doi.org/10.1143/jpsj.18.1174openalex-snapshot
Millimeter Wave Spectrum of Formaldehyde
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4173906openalex-extracted
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inferred← citeshttps://doi.org/10.1002/qua.21688openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/qua.22256openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/qua.22628openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4020-4853-1_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-011-9732-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-017-1048-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bpc.2009.03.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chemphys.2006.04.006openalex-snapshot
Theoretical study of Hal3CH/F2CD2 (Hal=F,Cl) and F3CH/FH heterodimers with blue shifted hydrogen bonds
inferred← citeshttps://doi.org/10.1016/j.chemphys.2006.06.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chemphys.2016.07.016openalex-snapshot
Blue-shift of the C-H stretching vibration in CHF3-H2O complex: Matrix isolation infrared spectroscopy and ab initio computations
inferred← citeshttps://doi.org/10.1016/j.comptc.2011.04.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2012.04.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2012.09.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2014.08.022openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2015.03.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2015.11.023openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2017.02.031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2019.05.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cplett.2006.10.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cplett.2010.02.054openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.10.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.10.026openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2010.01.065openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.09.049openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.theochem.2008.04.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.theochem.2008.04.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.theochem.2010.08.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.4c06690openalex-snapshot
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inferred← citeshttps://doi.org/10.11606/t.43.2006.tde-01122006-114239openalex-snapshot
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inferred← citeshttps://doi.org/10.15407/ujpe65.4.304openalex-snapshot
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Electrostatic Potential at Nuclei
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