Step-by-Step Replacement of Cyano Groups by Tricyanovinyls-The Influence on the Acidity
Acid-base properties are the simplest expression of compounds' coordinating ability. In the present work, we studied in silico how the gas-phase Brønsted acidity (GA) of several polycyano-substituted compounds change when cyano (CN) groups are replaced by 1,2,2-tricyanovinyl (TCNV) groups in (i...
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Published in | Molecules (Basel, Switzerland) Vol. 28; no. 24; p. 8157 |
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Format | Journal Article |
Language | English |
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01.12.2023
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Abstract | Acid-base properties are the simplest expression of compounds' coordinating ability. In the present work, we studied in silico how the gas-phase Brønsted acidity (GA) of several polycyano-substituted compounds change when cyano (CN) groups are replaced by 1,2,2-tricyanovinyl (TCNV) groups in (iso)cyanic acid, dicyanoamine, cyanoform, and hydrogen tetracyanoborate. Different tautomers and conformers/isomers are included in this study. Gas-phase acidity values are compared with the acidities of various acids, including percyanated protonated monocarba-
-dodecaborate (carborane acid) and dodecaborate, as well as hydrogen cyanide and 1,2,2-tricyanoethene. An estimation of acetonitrile (MeCN), dimethylsufoxide (DMSO), and 1,2-dichloroethane (DCE) acidities is presented using the COSMO-RS method and correlation analysis. The strongest acid with four TCNV groups shows remarkable acidic properties. |
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AbstractList | Acid-base properties are the simplest expression of compounds’ coordinating ability. In the present work, we studied in silico how the gas-phase Brønsted acidity (GA) of several polycyano-substituted compounds change when cyano (CN) groups are replaced by 1,2,2-tricyanovinyl (TCNV) groups in (iso)cyanic acid, dicyanoamine, cyanoform, and hydrogen tetracyanoborate. Different tautomers and conformers/isomers are included in this study. Gas-phase acidity values are compared with the acidities of various acids, including percyanated protonated monocarba-closo-dodecaborate (carborane acid) and dodecaborate, as well as hydrogen cyanide and 1,2,2-tricyanoethene. An estimation of acetonitrile (MeCN), dimethylsufoxide (DMSO), and 1,2-dichloroethane (DCE) acidities is presented using the COSMO-RS method and correlation analysis. The strongest acid with four TCNV groups shows remarkable acidic properties. Acid-base properties are the simplest expression of compounds' coordinating ability. In the present work, we studied in silico how the gas-phase Brønsted acidity (GA) of several polycyano-substituted compounds change when cyano (CN) groups are replaced by 1,2,2-tricyanovinyl (TCNV) groups in (iso)cyanic acid, dicyanoamine, cyanoform, and hydrogen tetracyanoborate. Different tautomers and conformers/isomers are included in this study. Gas-phase acidity values are compared with the acidities of various acids, including percyanated protonated monocarba- -dodecaborate (carborane acid) and dodecaborate, as well as hydrogen cyanide and 1,2,2-tricyanoethene. An estimation of acetonitrile (MeCN), dimethylsufoxide (DMSO), and 1,2-dichloroethane (DCE) acidities is presented using the COSMO-RS method and correlation analysis. The strongest acid with four TCNV groups shows remarkable acidic properties. |
Audience | Academic |
Author | Kütt, Agnes |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38138645$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1039/B816922E 10.1021/jo060031y 10.1002/celc.201701164 10.1039/B316122F 10.1021/ic048780q 10.1021/jo101409p 10.1002/aic.690480220 10.1134/S1070428008040179 10.1021/ja00418a040 10.1021/ja0255958 10.1002/ejoc.200500153 10.3390/molecules28248157 10.1002/poc.2946 10.1016/0013-4686(75)87002-2 10.1021/ja01544a055 10.1146/annurev-chembioeng-073009-100903 10.1016/j.tetlet.2018.08.054 10.1021/ct4003916 10.1021/ja01068a026 10.1021/jp2036108 10.1021/ar00156a004 10.1149/1.2943214 10.1002/9783527632220 10.1021/jp506485x 10.1021/j100007a062 10.1021/jo101581a 10.1002/cphc.200800305 10.1021/ja00969a029 10.1016/j.cplett.2020.138207 10.1021/jp905449k 10.1039/B713173A 10.1063/1.2770701 10.1002/jcc.21103 10.1016/j.tetlet.2004.09.146 10.1021/jo802641r 10.1002/anie.201506753 10.1002/ejoc.202001649 10.1016/j.theochem.2007.03.017 10.1002/(SICI)1521-3749(200002)626:2<560::AID-ZAAC560>3.0.CO;2-E 10.1021/jp980017s 10.1039/C7SC01424D |
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References | Lipping (ref_32) 2009; 113 Rodima (ref_3) 2011; 76 Vianello (ref_12) 2005; 2005 Curtiss (ref_29) 2007; 127 Tshepelevitsh (ref_33) 2021; 2021 Bernhardt (ref_20) 2005; 44 Paenurk (ref_36) 2017; 8 ref_30 Vianello (ref_11) 2004; 45 Ershov (ref_24) 2008; 44 Scheers (ref_21) 2008; 155 Raamat (ref_31) 2013; 26 Webster (ref_7) 1964; 86 Valadbeigi (ref_15) 2021; 763 ref_17 Angenendt (ref_22) 2011; 115 Middleton (ref_6) 1958; 80 Vianello (ref_10) 2008; 32 Klamt (ref_38) 1998; 102 Vianello (ref_9) 2009; 33 Gardner (ref_25) 1976; 98 Toomsalu (ref_28) 2013; 9 Webster (ref_5) 1966; 88 McCallum (ref_4) 1975; 20 Eckert (ref_39) 2002; 48 Klamt (ref_40) 2010; 1 Vianello (ref_8) 2010; 75 Ding (ref_34) 2009; 74 ref_46 Eckert (ref_41) 2009; 30 ref_45 Leito (ref_13) 2007; 815 ref_44 ref_43 Koppel (ref_27) 2002; 124 Bordwell (ref_35) 1988; 21 ref_1 Lipping (ref_16) 2015; 119 Selberg (ref_2) 2018; 59 Klamt (ref_37) 1995; 99 Soltner (ref_18) 2015; 54 Martins (ref_23) 2018; 5 ref_26 Bernhardt (ref_19) 2000; 626 Leito (ref_42) 2006; 71 Koppel (ref_14) 2009; 10 |
References_xml | – volume: 33 start-page: 739 year: 2009 ident: ref_9 article-title: The Engineering of Powerful Non-Ionic Superacids in Silico—A DFT-B3LYP Study of Open Chain Polycyanopolyenes publication-title: New J. Chem. doi: 10.1039/B816922E contributor: fullname: Vianello – ident: ref_30 – volume: 71 start-page: 2829 year: 2006 ident: ref_42 article-title: A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile publication-title: J. Org. Chem. doi: 10.1021/jo060031y contributor: fullname: Leito – volume: 5 start-page: 598 year: 2018 ident: ref_23 article-title: Improved Performance of Ionic Liquid Supercapacitors by Using Tetracyanoborate Anions publication-title: ChemElectroChem doi: 10.1002/celc.201701164 contributor: fullname: Martins – ident: ref_17 doi: 10.1039/B316122F – volume: 44 start-page: 1015 year: 2005 ident: ref_20 article-title: Tetracyanoborate Salts M[B(CN)4] with M = Singly Charged Cations: Properties and Structures publication-title: Inorg. Chem. doi: 10.1021/ic048780q contributor: fullname: Bernhardt – volume: 76 start-page: 391 year: 2011 ident: ref_3 article-title: Equilibrium Acidities of Superacids publication-title: J. Org. Chem. doi: 10.1021/jo101409p contributor: fullname: Rodima – volume: 48 start-page: 369 year: 2002 ident: ref_39 article-title: Fast Solvent Screening via Quantum Chemistry: COSMO-RS Approach publication-title: AIChE J. doi: 10.1002/aic.690480220 contributor: fullname: Eckert – volume: 44 start-page: 570 year: 2008 ident: ref_24 article-title: Three-Component Synthesis of 2-(4-Amino-2,5-Dihydro-1H-Imidazol-5-Ylidene)Malononitriles publication-title: Russ. J. Org. Chem. doi: 10.1134/S1070428008040179 contributor: fullname: Ershov – volume: 98 start-page: 558 year: 1976 ident: ref_25 article-title: Alkylation of Tetracyanoethylene. Reaction with Grignard Reagents publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00418a040 contributor: fullname: Gardner – volume: 124 start-page: 5594 year: 2002 ident: ref_27 article-title: Generalized Principle of Designing Neutral Superstrong Brønsted Acids publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0255958 contributor: fullname: Koppel – volume: 2005 start-page: 3571 year: 2005 ident: ref_12 article-title: Strong Acidity of Some Polycyclic Aromatic Compounds Annulated to a Cyclopentadiene Moiety and Their Cyano Derivatives—A Density Functional B3LYP Study publication-title: Eur. J. Org. Chem. doi: 10.1002/ejoc.200500153 contributor: fullname: Vianello – ident: ref_26 doi: 10.3390/molecules28248157 – ident: ref_44 – volume: 26 start-page: 162 year: 2013 ident: ref_31 article-title: Acidities of Strong Neutral Brønsted Acids in Different Media publication-title: J. Phys. Org. Chem. doi: 10.1002/poc.2946 contributor: fullname: Raamat – volume: 20 start-page: 815 year: 1975 ident: ref_4 article-title: Conductance of Acids in Dimethyl-Sulphoxide—II. Conductance of Some Strong Acids in DMSO at 25 °C publication-title: Electrochim. Acta doi: 10.1016/0013-4686(75)87002-2 contributor: fullname: McCallum – volume: 80 start-page: 2795 year: 1958 ident: ref_6 article-title: Cyanocarbon Chemistry. V.1 Cyanocarbon Acids and Their Salts publication-title: J. Am. Chem. Soc. doi: 10.1021/ja01544a055 contributor: fullname: Middleton – volume: 1 start-page: 101 year: 2010 ident: ref_40 article-title: COSMO-RS: An Alternative to Simulation for Calculating Thermodynamic Properties of Liquid Mixtures publication-title: Annu. Rev. Chem. Biomol. Eng. doi: 10.1146/annurev-chembioeng-073009-100903 contributor: fullname: Klamt – volume: 59 start-page: 3738 year: 2018 ident: ref_2 article-title: pKa Values in Organic Chemistry—Making Maximum Use of the Available Data publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2018.08.054 contributor: fullname: Selberg – volume: 9 start-page: 3947 year: 2013 ident: ref_28 article-title: Critical Test of Some Computational Chemistry Methods for Prediction of Gas-Phase Acidities and Basicities publication-title: J. Chem. Theory Comput. doi: 10.1021/ct4003916 contributor: fullname: Toomsalu – volume: 86 start-page: 2898 year: 1964 ident: ref_7 article-title: Hexacyanobutadiene publication-title: J. Am. Chem. Soc. doi: 10.1021/ja01068a026 contributor: fullname: Webster – volume: 115 start-page: 7808 year: 2011 ident: ref_22 article-title: Ionic Liquid Based Lithium Battery Electrolytes: Charge Carriers and Interactions Derived by Density Functional Theory Calculations publication-title: J. Phys. Chem. B doi: 10.1021/jp2036108 contributor: fullname: Angenendt – volume: 21 start-page: 456 year: 1988 ident: ref_35 article-title: Equilibrium Acidities in Dimethyl Sulfoxide Solution publication-title: Acc. Chem. Res. doi: 10.1021/ar00156a004 contributor: fullname: Bordwell – volume: 155 start-page: A628 year: 2008 ident: ref_21 article-title: Anions for Lithium Battery Electrolytes: A Spectroscopic and Theoretical Study of the B (CN)4− Anion of the Ionic Liquid C2mim [B(CN)4] publication-title: J. Electrochem. Soc. doi: 10.1149/1.2943214 contributor: fullname: Scheers – ident: ref_46 – ident: ref_1 doi: 10.1002/9783527632220 – volume: 119 start-page: 735 year: 2015 ident: ref_16 article-title: Superacidity of Closo-Dodecaborate-Based Brønsted Acids: A DFT Study publication-title: J. Phys. Chem. A doi: 10.1021/jp506485x contributor: fullname: Lipping – volume: 99 start-page: 2224 year: 1995 ident: ref_37 article-title: Conductor-like Screening Model for Real Solvents: A New Approach to the Quantitative Calculation of Solvation Phenomena publication-title: J. Phys. Chem. doi: 10.1021/j100007a062 contributor: fullname: Klamt – volume: 75 start-page: 7670 year: 2010 ident: ref_8 article-title: Polycyano Derivatives of Some Organic Tri- and Hexacyclic Molecules Are Powerful Super- and Hyperacids in the Gas Phase and DMSO: Computational Study by DFT Approach publication-title: J. Org. Chem. doi: 10.1021/jo101581a contributor: fullname: Vianello – volume: 10 start-page: 499 year: 2009 ident: ref_14 article-title: Boratabenzene Anions C5B(CN)6− and C5B(CF3)6− and the Superacidic Properties of Their Conjugate Acids publication-title: ChemPhysChem doi: 10.1002/cphc.200800305 contributor: fullname: Koppel – volume: 88 start-page: 4055 year: 1966 ident: ref_5 article-title: Diazotetracyanocyclopentadiene1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00969a029 contributor: fullname: Webster – volume: 763 start-page: 138207 year: 2021 ident: ref_15 article-title: Organometallic Superacids and Hyperacids: Acidity Enhancement by Internal Bonding with a Strong Electron-Pair Acceptor Group BX2 publication-title: Chem. Phys. Lett. doi: 10.1016/j.cplett.2020.138207 contributor: fullname: Valadbeigi – volume: 113 start-page: 12972 year: 2009 ident: ref_32 article-title: Gas-Phase Brønsted Superacidity of Some Derivatives of Monocarba-Closo-Borates: A Computational Study publication-title: J. Phys. Chem. A doi: 10.1021/jp905449k contributor: fullname: Lipping – volume: 32 start-page: 413 year: 2008 ident: ref_10 article-title: Rees Polycyanated Hydrocarbons and Related Compounds Are Extremely Powerful Brønsted Superacids in the Gas-Phase and DMSO—A Density Functional B3LYP Study publication-title: New J. Chem. doi: 10.1039/B713173A contributor: fullname: Vianello – volume: 127 start-page: 124105 year: 2007 ident: ref_29 article-title: Gaussian-4 Theory Using Reduced Order Perturbation Theory publication-title: J. Chem. Phys. doi: 10.1063/1.2770701 contributor: fullname: Curtiss – volume: 30 start-page: 799 year: 2009 ident: ref_41 article-title: Prediction of Acidity in Acetonitrile Solution with COSMO-RS publication-title: J. Comput. Chem. doi: 10.1002/jcc.21103 contributor: fullname: Eckert – ident: ref_45 – volume: 45 start-page: 8663 year: 2004 ident: ref_11 article-title: Extending the Acidity Ladder of Neutral Organic Superacids—A DFT-B3LYP Study of Deprotonation of Nonacyanofluorene publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2004.09.146 contributor: fullname: Vianello – volume: 74 start-page: 2679 year: 2009 ident: ref_34 article-title: First-Principles Calculation of pKa Values for Organic Acids in Nonaqueous Solution publication-title: J. Org. Chem. doi: 10.1021/jo802641r contributor: fullname: Ding – ident: ref_43 – volume: 54 start-page: 13775 year: 2015 ident: ref_18 article-title: The Existence of Tricyanomethane publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201506753 contributor: fullname: Soltner – volume: 2021 start-page: 1407 year: 2021 ident: ref_33 article-title: Strengths of Acids in Acetonitrile publication-title: Eur. J. Org. Chem. doi: 10.1002/ejoc.202001649 contributor: fullname: Tshepelevitsh – volume: 815 start-page: 41 year: 2007 ident: ref_13 article-title: Anions N[C(CN)2]3− and P[C(CN)2]3− and the Superacidic Properties of Their Conjugate Acids publication-title: THEOCHEM-J. Mol. Struc. doi: 10.1016/j.theochem.2007.03.017 contributor: fullname: Leito – volume: 626 start-page: 560 year: 2000 ident: ref_19 article-title: Die Tetracyanoborate M[B(CN)4], M = [Bu4N]+, Ag+, K+ publication-title: Z. Anorg. Allg. Chem. doi: 10.1002/(SICI)1521-3749(200002)626:2<560::AID-ZAAC560>3.0.CO;2-E contributor: fullname: Bernhardt – volume: 102 start-page: 5074 year: 1998 ident: ref_38 article-title: Refinement and Parametrization of COSMO-RS publication-title: J. Phys. Chem. A doi: 10.1021/jp980017s contributor: fullname: Klamt – volume: 8 start-page: 6964 year: 2017 ident: ref_36 article-title: A Unified View to Brønsted Acidity Scales: Do We Need Solvated Protons? publication-title: Chem. Sci. doi: 10.1039/C7SC01424D contributor: fullname: Paenurk |
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SubjectTerms | Acetonitrile acid-base properties Comparative analysis COSMO-RS cyanocarbon acids gas-phase acidity Hydrogen Hydrogen-ion concentration polycyano compounds Solvents tricyanovinyl |
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Title | Step-by-Step Replacement of Cyano Groups by Tricyanovinyls-The Influence on the Acidity |
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