Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 48 checked references that resolve
resolves10.1021/jp052384rCyclodehydrogenation Reactions to Cyclopentafused Polycyclic Aromatic Hydrocarbons
resolves10.1021/jp906541aDetailed Kinetic Monte Carlo Simulations of Graphene-Edge Growth
resolves10.1039/C4CP00112EStochastic atomistic simulation of polycyclic aromatic hydrocarbon growth in combustion
resolves10.1016/j.proci.2012.07.030Thermodynamics of poly-aromatic hydrocarbon clustering and the effects of substituted aliphatic chains
resolves10.1039/c2cp23008aA quantitative study of the clustering of polycyclic aromatic hydrocarbons at high temperatures
resolves10.1039/b104056cThermodynamic and kinetic issues in the formation and oxidation of aromatic species
resolves10.1039/C6FD00111DPressure-dependent rate constants for PAH growth: formation of indene and its conversion to naphthalene
resolves10.1021/jp067135xAb Initio G3-type/Statistical Theory Study of the Formation of Indene in Combustion Flames. I. Pathways Involving Benzene and Phenyl Radical
resolves10.1016/j.combustflame.2010.03.008A lean methane premixed laminar flame doped with components of diesel fuel part III: Indane and comparison between n-butylbenzene, n-propylcyclohexane and indane
resolves10.1039/C9CP02930CHow to add a five-membered ring to polycyclic aromatic hydrocarbons (PAHs) – molecular mass growth of the 2-naphthyl radical (C
<sub>10</sub>
H
<sub>7</sub>
) to benzindenes (C
<sub>13</sub>
H
<sub>10</sub>
) as a case study
resolves10.1063/1.464913Density-functional thermochemistry. III. The role of exact exchange
resolves10.1063/1.478676Gaussian-3 theory using density functional geometries and zero-point energies
resolves10.1021/jp511403aBenchmarking Compound Methods (CBS-QB3, CBS-APNO, G3, G4, W1BD) against the Active Thermochemical Tables: A Litmus Test for Cost-Effective Molecular Formation Enthalpies
resolves10.1021/acs.jpca.5b05448Benchmarking Compound Methods (CBS-QB3, CBS-APNO, G3, G4, W1BD) against the Active Thermochemical Tables: Formation Enthalpies of Radicals
resolves10.1063/1.477422Gaussian-3 (G3) theory for molecules containing first and second-row atoms
resolves10.1021/jp3051033MESMER: An Open-Source Master Equation Solver for Multi-Energy Well Reactions
resolves10.1021/ja00517a004Tunneling corrections to unimolecular rate constants, with application to formaldehyde
resolves10.1063/1.475616Identification and treatment of internal rotation in normal mode vibrational analysis
resolves10.1002/kin.1017Multiple‐Well, multiple‐path unimolecular reaction systems. I. MultiWell computer program suite
resolves10.1021/ct0500491Hydrogen Abstraction Acetylene Addition and Diels−Alder Mechanisms of PAH Formation: A Detailed Study Using First Principles Calculations
resolves10.1021/jo00073a058Synthesis of methylene-bridged polycyclic aromatic hydrocarbons: an efficient, double Friedel-Crafts cyclization approach to 11H-benz[bc]aceanthrylene
resolves10.1021/jo0100603First Examples of Stable Arenium Ions from Large Methylene-Bridged Polycyclic Aromatic Hydrocarbons (PAHs). Directive Effects and Charge Delocalization Mode
resolves10.1093/carcin/9.12.2275Comparative tumor-initiating activity of methylene-bridged and bay-region methylated derivatives of benz[<i>a</i>]anthracene and chrysene
resolves10.1021/ef010263uYields of Polycyclic Aromatic Hydrocarbons from the Pyrolysis of Catechol [<i>o</i><i>rtho</i>-Dihydroxybenzene]: Temperature and Residence Time Effects
resolves10.1080/10406630701462940UV SPECTRAL IDENTIFICATION OF POLYCYCLIC AROMATIC HYDROCARBON PRODUCTS OF SUPERCRITICAL 1-METHYLNAPHTHALENE PYROLYSIS
resolves10.1021/jp071813dIn Situ Direct Sampling Mass Spectrometric Study on Formation of Polycyclic Aromatic Hydrocarbons in Toluene Pyrolysis
resolves10.1039/b919644gA highly efficient growth mechanism of polycyclic aromatic hydrocarbons
resolves10.1016/j.combustflame.2017.09.005Reaction mechanism, rate constants, and product yields for the oxidation of Cyclopentadienyl and embedded five-member ring radicals with hydroxyl
resolves10.1016/j.combustflame.2017.10.012Detailed, sterically-resolved modeling of soot oxidation: Role of O atoms, interplay with particle nanostructure, and emergence of inner particle burning
The 5 references without a DOI — listed, not checked
no DOI — not checkedFrisch MJ, Trucks GW, Schlegel HB, et al., Gaussian 09.
no DOI — not checked10.1016/j.fuel.2020.119023_b0135
no DOI — not checked10.1016/j.fuel.2020.119023_b0160
no DOI — not checkedLindstedt R, Waldheim B, Robinson R, in: 8th International Symposium Towards Cleaner Diesel Engines 2011, Shell Global Solutions (UK), Chester, 2011, p. 36.
no DOI — not checkedReaction Design, CHEMKIN-PRO 15112, San Diego, 2011.
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