메뉴 건너뛰기




Volumn 118, Issue 21, 2014, Pages 3835-3845

Substituent effects in the noncovalent bonding of SO2 to molecules containing a carbonyl group. The dominating role of the chalcogen bond

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; SULFUR DIOXIDE;

EID: 84901649703     PISSN: 10895639     EISSN: 15205215     Source Type: Journal    
DOI: 10.1021/jp501932g     Document Type: Article
Times cited : (49)

References (62)
  • 2
    • 77954598483 scopus 로고    scopus 로고
    • The Halogen Bond: An Interim Perspective
    • Legon, A. C. The Halogen Bond: An Interim Perspective Phys. Chem. Chem. Phys. 2010, 12, 7736-7747
    • (2010) Phys. Chem. Chem. Phys. , vol.12 , pp. 7736-7747
    • Legon, A.C.1
  • 3
    • 84859761485 scopus 로고    scopus 로고
    • Halogen Bonding in Solution
    • Erdelyi, M. Halogen Bonding in Solution Chem. Soc. Rev. 2012, 41, 3547-3557
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 3547-3557
    • Erdelyi, M.1
  • 4
    • 84876717733 scopus 로고    scopus 로고
    • Sensitivity of Noncovalent Bonds to Intermolecular Separation: Hydrogen, Halogen, Chalcogen, and Pnicogen Bonds
    • Scheiner, S. Sensitivity of Noncovalent Bonds to Intermolecular Separation: Hydrogen, Halogen, Chalcogen, and Pnicogen Bonds CrystEngComm 2013, 15, 3119-3124
    • (2013) CrystEngComm , vol.15 , pp. 3119-3124
    • Scheiner, S.1
  • 5
    • 84887976814 scopus 로고    scopus 로고
    • Experimental Characterization of C-X···Y-C (X = Br, I; Y = F, Cl) Halogen-Halogen Bonds
    • Hauchecorne, D.; Herrebout, W. A. Experimental Characterization of C-X···Y-C (X = Br, I; Y = F, Cl) Halogen-Halogen Bonds J. Phys. Chem. A 2013, 117, 11548-11557
    • (2013) J. Phys. Chem. A , vol.117 , pp. 11548-11557
    • Hauchecorne, D.1    Herrebout, W.A.2
  • 6
    • 84888294131 scopus 로고    scopus 로고
    • Halogen Bond Tunability II: The Varying Roles of Electrostatic and Dispersion Contributions to Attraction in Halogen Bonds
    • Riley, K.; Murray, J.; Fanfrlík, J.; Rezác, J.; Solá, R.; Concha, M.; Ramos, F.; Politzer, P. Halogen Bond Tunability II: The Varying Roles of Electrostatic and Dispersion Contributions to Attraction in Halogen Bonds J. Mol. Model. 2013, 19, 4651-4659
    • (2013) J. Mol. Model. , vol.19 , pp. 4651-4659
    • Riley, K.1    Murray, J.2    Fanfrlík, J.3    Rezác, J.4    Solá, R.5    Concha, M.6    Ramos, F.7    Politzer, P.8
  • 7
    • 84883721736 scopus 로고    scopus 로고
    • Cl···Cl Interactions in Molecular Crystals: Insights from the Theoretical Charge Density Analysis
    • Vener, M. V.; Shishkina, A. V.; Rykounov, A. A.; Tsirelson, V. G. Cl···Cl Interactions in Molecular Crystals: Insights from the Theoretical Charge Density Analysis J. Phys. Chem. A 2013, 117, 8459-8467
    • (2013) J. Phys. Chem. A , vol.117 , pp. 8459-8467
    • Vener, M.V.1    Shishkina, A.V.2    Rykounov, A.A.3    Tsirelson, V.G.4
  • 8
    • 84879762677 scopus 로고    scopus 로고
    • Substituent Effects on the Cooperativity of Halogen Bonding
    • Solimannejad, M.; Malekani, M.; Alkorta, I. Substituent Effects on the Cooperativity of Halogen Bonding J. Phys. Chem. A 2013, 117, 5551-5557
    • (2013) J. Phys. Chem. A , vol.117 , pp. 5551-5557
    • Solimannejad, M.1    Malekani, M.2    Alkorta, I.3
  • 9
    • 84877261230 scopus 로고    scopus 로고
    • Are Halogen Bonded Structures Electrostatically Driven?
    • Stone, A. J. Are Halogen Bonded Structures Electrostatically Driven? J. Am. Chem. Soc. 2013, 135, 7005-7009
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 7005-7009
    • Stone, A.J.1
  • 13
    • 80052514867 scopus 로고    scopus 로고
    • Prediction of a New Delocalised Bonding Motif between Group 15 or Group 16 Atoms
    • Bühl, M.; Kilian, P.; Woollins, J. D. Prediction of a New Delocalised Bonding Motif between Group 15 or Group 16 Atoms ChemPhysChem 2011, 12, 2405-2408
    • (2011) ChemPhysChem , vol.12 , pp. 2405-2408
    • Bühl, M.1    Kilian, P.2    Woollins, J.D.3
  • 14
    • 79952494920 scopus 로고    scopus 로고
    • A New Noncovalent Force: Comparison of P···N Interaction with Hydrogen and Halogen Bonds
    • Scheiner, S. A New Noncovalent Force: Comparison of P·· ·N Interaction with Hydrogen and Halogen Bonds J. Chem. Phys. 2011, 134, 094315
    • (2011) J. Chem. Phys. , vol.134 , pp. 094315
    • Scheiner, S.1
  • 15
    • 80052033913 scopus 로고    scopus 로고
    • Effects of Substituents upon the P···N Noncovalent Interaction: The Limits of Its Strength
    • Scheiner, S. Effects of Substituents upon the P···N Noncovalent Interaction: The Limits of Its Strength J. Phys. Chem. A 2011, 115, 11202-11209
    • (2011) J. Phys. Chem. A , vol.115 , pp. 11202-11209
    • Scheiner, S.1
  • 16
    • 84861576672 scopus 로고    scopus 로고
    • Effects of Carbon Chain Substituents on the P···N Noncovalent Bond
    • Adhikari, U.; Scheiner, S. Effects of Carbon Chain Substituents on the P···N Noncovalent Bond Chem. Phys. Lett. 2012, 536, 30-33
    • (2012) Chem. Phys. Lett. , vol.536 , pp. 30-33
    • Adhikari, U.1    Scheiner, S.2
  • 20
    • 84874102873 scopus 로고    scopus 로고
    • The Pnicogen Bond: Its Relation to Hydrogen, Halogen, and Other Noncovalent Bonds
    • Scheiner, S. The Pnicogen Bond: Its Relation to Hydrogen, Halogen, and Other Noncovalent Bonds Acc. Chem. Res. 2012, 46, 280-288
    • (2012) Acc. Chem. Res. , vol.46 , pp. 280-288
    • Scheiner, S.1
  • 21
    • 0032495790 scopus 로고    scopus 로고
    • Intramolecular nonbonded S···O interaction recognized in (acylimino)thiadiazoline derivatives as angiotensin II receptor antagonists and related compounds
    • DOI 10.1021/ja973109o
    • Nagao, Y.; Hirata, T.; Goto, S.; Sano, S.; Kakehi, A.; Iizuka, K.; Shiro, M. Intramolecular Nonbonded S···O Interaction Recognized in (Acylimino)thiadiazoline Derivatives as Angiotensin II Receptor Antagonists and Related Compounds J. Am. Chem. Soc. 1998, 120, 3104-3110 (Pubitemid 28204523)
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.13 , pp. 3104-3110
    • Nagao, Y.1    Hirata, T.2    Goto, S.3    Sano, S.4    Kakehi, A.5    Iizuka, K.6    Shiro, M.7
  • 22
    • 0037019551 scopus 로고    scopus 로고
    • Statistical and theoretical investigations on the directionality of nonbonded S···O interactions. Implications for molecular design and protein engineering
    • DOI 10.1021/ja026472q
    • Iwaoka, M.; Takemoto, S.; Tomoda, S. Statistical and Theoretical Investigations on the Directionality of Nonbonded S···O Interactions. Implications for Molecular Design and Protein Engineering J. Am. Chem. Soc. 2002, 124, 10613-10620 (Pubitemid 34977414)
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.35 , pp. 10613-10620
    • Iwaoka, M.1    Takemoto, S.2    Tomoda, S.3
  • 23
    • 0037063541 scopus 로고    scopus 로고
    • Nanotube Formation Favored by Chalcogen-Chalcogen Interactions
    • Werz, D. B.; Gleiter, R.; Rominger, F. Nanotube Formation Favored by Chalcogen-Chalcogen Interactions J. Am. Chem. Soc. 2002, 124, 10638-10639
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10638-10639
    • Werz, D.B.1    Gleiter, R.2    Rominger, F.3
  • 24
    • 0041845060 scopus 로고    scopus 로고
    • Characterization of Intramolecular Hydrogen Bonds and Competitive Chalcogen-Chalcogen Interactions on the Basis of the Topology of the Charge Density
    • Sanz, P.; Mo, O.; Yanez, M. Characterization of Intramolecular Hydrogen Bonds and Competitive Chalcogen-Chalcogen Interactions on the Basis of the Topology of the Charge Density Phys. Chem. Chem. Phys. 2003, 5, 2942-2947
    • (2003) Phys. Chem. Chem. Phys. , vol.5 , pp. 2942-2947
    • Sanz, P.1    Mo, O.2    Yanez, M.3
  • 25
    • 33644654429 scopus 로고    scopus 로고
    • Theoretical investigations on chalcogen-chalcogen interactions: What makes these nonbonded interactions bonding?
    • DOI 10.1021/ja056827g
    • Bleiholder, C.; Werz, D. B.; Köppel, H.; Gleiter, R. Theoretical Investigations on Chalcogen-Chalcogen Interactions: What Makes These Nonbonded Interactions Bonding? J. Am. Chem. Soc. 2006, 128, 2666-2674 (Pubitemid 43327946)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.8 , pp. 2666-2674
    • Bleiholder, C.1    Werz, D.B.2    Koppel, H.3    Gleiter, R.4
  • 26
    • 80051584636 scopus 로고    scopus 로고
    • Theoretical and Crystallographic Data Investigations of Noncovalent S···O Interactions
    • Junming, L.; Yunxiang, L.; Subin, Y.; Weiliang, Z. Theoretical and Crystallographic Data Investigations of Noncovalent S···O Interactions Struct. Chem. 2011, 22, 757-763
    • (2011) Struct. Chem. , vol.22 , pp. 757-763
    • Junming, L.1    Yunxiang, L.2    Subin, Y.3    Weiliang, Z.4
  • 27
    • 84859156862 scopus 로고    scopus 로고
    • Sensitivity of Pnicogen, Chalcogen, Halogen and H-Bonds to Angular Distortions
    • Adhikari, U.; Scheiner, S. Sensitivity of Pnicogen, Chalcogen, Halogen and H-Bonds to Angular Distortions Chem. Phys. Lett. 2012, 532, 31-35
    • (2012) Chem. Phys. Lett. , vol.532 , pp. 31-35
    • Adhikari, U.1    Scheiner, S.2
  • 28
    • 84856387510 scopus 로고    scopus 로고
    • Intermolecular Weak Interactions in HTeXH Dimers (X - O, S, Se, Te): Hydrogen Bonds, Chalcogen-Chalcogen Contacts and Chiral Discrimination
    • Sánchez-Sanz, G.; Trujillo, C.; Alkorta, I.; Elguero, J. Intermolecular Weak Interactions in HTeXH Dimers (X - O, S, Se, Te): Hydrogen Bonds, Chalcogen-Chalcogen Contacts and Chiral Discrimination ChemPhysChem 2012, 13, 496-503
    • (2012) ChemPhysChem , vol.13 , pp. 496-503
    • Sánchez-Sanz, G.1    Trujillo, C.2    Alkorta, I.3    Elguero, J.4
  • 29
    • 84862996200 scopus 로고    scopus 로고
    • Hypervalent Nonbonded Interactions of a Divalent Sulfur Atom. Implications in Protein Architecture and the Functions
    • Iwaoka, M.; Isozumi, N. Hypervalent Nonbonded Interactions of a Divalent Sulfur Atom. Implications in Protein Architecture and the Functions Molecules 2012, 17, 7266-7283
    • (2012) Molecules , vol.17 , pp. 7266-7283
    • Iwaoka, M.1    Isozumi, N.2
  • 30
    • 84873592899 scopus 로고    scopus 로고
    • Molecular Evidence for the Intermolecular SS Interaction in the Surface Molecular Packing Motifs of a Fused Thiophene Derivative
    • Wang, X.-Y.; Jiang, W.; Chen, T.; Yan, H.-J.; Wang, Z.-H.; Wan, L.-J.; Wang, D. Molecular Evidence for the Intermolecular SS Interaction in the Surface Molecular Packing Motifs of a Fused Thiophene Derivative Chem. Commun. 2013, 49, 1829-1831
    • (2013) Chem. Commun. , vol.49 , pp. 1829-1831
    • Wang, X.-Y.1    Jiang, W.2    Chen, T.3    Yan, H.-J.4    Wang, Z.-H.5    Wan, L.-J.6    Wang, D.7
  • 31
    • 84876711132 scopus 로고    scopus 로고
    • Halogen Bonding versus Chalcogen and Pnicogen Bonding: A Combined Cambridge Structural Database and Theoretical Study
    • Bauza, A.; Quinonero, D.; Deya, P. M.; Frontera, A. Halogen Bonding versus Chalcogen and Pnicogen Bonding: A Combined Cambridge Structural Database and Theoretical Study CrystEngComm 2013, 15, 3137-3144
    • (2013) CrystEngComm , vol.15 , pp. 3137-3144
    • Bauza, A.1    Quinonero, D.2    Deya, P.M.3    Frontera, A.4
  • 32
    • 84887519675 scopus 로고    scopus 로고
    • Tetrel-Bonding Interaction: Rediscovered Supramolecular Force?
    • Bauzá, A.; Mooibroek, T. J.; Frontera, A. Tetrel-Bonding Interaction: Rediscovered Supramolecular Force? Angew. Chem., Int. Ed. 2013, 52, 12317-12321
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 12317-12321
    • Bauzá, A.1    Mooibroek, T.J.2    Frontera, A.3
  • 33
    • 84881394565 scopus 로고    scopus 로고
    • The X-CY (X = O/F, y = O/S/F/Cl/Br/N/P) Carbon Bond and Hydrophobic Interactions
    • Mani, D.; Arunan, E. The X-CY (X = O/F, Y = O/S/F/Cl/Br/N/P) Carbon Bond and Hydrophobic Interactions Phys. Chem. Chem. Phys. 2013, 15, 14377-14383
    • (2013) Phys. Chem. Chem. Phys. , vol.15 , pp. 14377-14383
    • Mani, D.1    Arunan, E.2
  • 37
    • 84893338021 scopus 로고    scopus 로고
    • 2 Molecules (n = 1, 2, 3) with Formaldehyde and Thioformaldehyde
    • 2 Molecules (n = 1, 2, 3) with Formaldehyde and Thioformaldehyde J. Chem. Phys. 2014, 140, 034302
    • (2014) J. Chem. Phys. , vol.140 , pp. 034302
    • Azofra, L.M.1    Scheiner, S.2
  • 38
    • 84857801456 scopus 로고    scopus 로고
    • σ-Holes, π-Holes and Electrostatically-driven Interactions
    • Murray, J.; Lane, P.; Clark, T.; Riley, K.; Politzer, P. σ-Holes, π-Holes and Electrostatically-driven Interactions J. Mol. Model. 2012, 18, 541-548
    • (2012) J. Mol. Model. , vol.18 , pp. 541-548
    • Murray, J.1    Lane, P.2    Clark, T.3    Riley, K.4    Politzer, P.5
  • 41
    • 6944251055 scopus 로고
    • Note on an Approximation Treatment for Many-Electron Systems
    • Møller, C.; Plesset, M. S. Note on an Approximation Treatment for Many-Electron Systems Phys. Rev. 1934, 46, 618-622
    • (1934) Phys. Rev. , vol.46 , pp. 618-622
    • Møller, C.1    Plesset, M.S.2
  • 42
    • 36749105379 scopus 로고
    • Gaussian Basis Sets for the Atoms Gallium through Krypton
    • Dunning, T. H. Gaussian Basis Sets for the Atoms Gallium through Krypton J. Chem. Phys. 1977, 66, 1382-1383
    • (1977) J. Chem. Phys. , vol.66 , pp. 1382-1383
    • Dunning, T.H.1
  • 43
    • 33746614482 scopus 로고
    • Gaussian Basis Sets for Use in Correlated Molecular Calculations. I. The Atoms Boron Through Neon and Hydrogen
    • Dunning, T. H. J. Gaussian Basis Sets for Use in Correlated Molecular Calculations. I. The Atoms Boron Through Neon and Hydrogen J. Chem. Phys. 1989, 90, 1007-1023
    • (1989) J. Chem. Phys. , vol.90 , pp. 1007-1023
    • Dunning, T.H.J.1
  • 44
    • 3843146349 scopus 로고
    • Gaussian Basis Sets for Use in Correlated Molecular Calculations. III. The Atoms Aluminum through Argon
    • Woon, D. E.; Dunning, T. H. Gaussian Basis Sets for Use in Correlated Molecular Calculations. III. The Atoms Aluminum through Argon J. Chem. Phys. 1993, 98, 1358-1371
    • (1993) J. Chem. Phys. , vol.98 , pp. 1358-1371
    • Woon, D.E.1    Dunning, T.H.2
  • 50
    • 55849117399 scopus 로고    scopus 로고
    • Long-range Corrected Hybrid Density Functionals with Damped Atom-Atom Dispersion Corrections
    • Chai, J.-D.; Head-Gordon, M. Long-range Corrected Hybrid Density Functionals with Damped Atom-Atom Dispersion Corrections Phys. Chem. Chem. Phys. 2008, 10, 6615-6620
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 6615-6620
    • Chai, J.-D.1    Head-Gordon, M.2
  • 51
    • 84865050335 scopus 로고    scopus 로고
    • TK Gristmill Software, Overland Park, KS, USA
    • Keith, T. A. AIMA11; TK Gristmill Software, Overland Park, KS, USA, 2013.
    • (2013) AIMA11
    • Keith, T.A.1
  • 53
    • 47249165244 scopus 로고    scopus 로고
    • σ-Hole Bonding between Like Atoms; A Fallacy of Atomic Charges
    • Politzer, P.; Murray, J.; Concha, M. σ-Hole Bonding between Like Atoms; A Fallacy of Atomic Charges J. Mol. Model. 2008, 14, 659-665
    • (2008) J. Mol. Model. , vol.14 , pp. 659-665
    • Politzer, P.1    Murray, J.2    Concha, M.3
  • 54
    • 0004592759 scopus 로고
    • Characterization of C-H-O Hydrogen-Bonds on the Basis of the Charge-Density
    • Koch, U.; Popelier, P. L. A. Characterization of C-H-O Hydrogen-Bonds on the Basis of the Charge-Density J. Phys. Chem. 1995, 99, 9747-9754
    • (1995) J. Phys. Chem. , vol.99 , pp. 9747-9754
    • Koch, U.1    Popelier, P.L.A.2
  • 55
    • 84865049096 scopus 로고    scopus 로고
    • Conformational Study of the Open-Chain and Furanose Structures of D-Erythrose and D-Threose
    • Azofra, L. M.; Alkorta, I.; Elguero, J.; Popelier, P. L. A. Conformational Study of the Open-Chain and Furanose Structures of D-Erythrose and D-Threose Carbohydr. Res. 2012, 358, 96-105
    • (2012) Carbohydr. Res. , vol.358 , pp. 96-105
    • Azofra, L.M.1    Alkorta, I.2    Elguero, J.3    Popelier, P.L.A.4
  • 56
    • 84891358744 scopus 로고    scopus 로고
    • Conformational Preference and Chiroptical Response of Carbohydrates D-Ribose and 2-Deoxy-D-ribose in Aqueous and Solid Phases
    • Quesada-Moreno, M. M.; Azofra, L. M.; Avilés-Moreno, J. R.; Alkorta, I.; Elguero, J.; López-González, J. J. Conformational Preference and Chiroptical Response of Carbohydrates D-Ribose and 2-Deoxy-D-ribose in Aqueous and Solid Phases J. Phys. Chem. B 2013, 117, 14599-14614
    • (2013) J. Phys. Chem. B , vol.117 , pp. 14599-14614
    • Quesada-Moreno, M.M.1    Azofra, L.M.2    Avilés-Moreno, J.R.3    Alkorta, I.4    Elguero, J.5    López-González, J.J.6
  • 58
    • 80051913945 scopus 로고    scopus 로고
    • Halogen Bond Involving Hypervalent Halogen: CSD Search and Theoretical Study
    • Wang, W. Halogen Bond Involving Hypervalent Halogen: CSD Search and Theoretical Study J. Phys. Chem. A 2011, 115, 9294-9299
    • (2011) J. Phys. Chem. A , vol.115 , pp. 9294-9299
    • Wang, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.