Soft experimental constraints for soft interactions: a spectroscopic benchmark data set for weak and strong hydrogen bonds

被引:21
|
作者
Oswald, Soenke [1 ]
Suhm, Martin A. [1 ]
机构
[1] Univ Gottingen, Inst Phys Chem, Tammannstr 6, D-37077 Gottingen, Germany
关键词
DENSITY-FUNCTIONAL THEORY; MAIN-GROUP THERMOCHEMISTRY; MICROWAVE-SPECTRUM; NONCOVALENT INTERACTIONS; INTERNAL-ROTATION; FORMIC-ACID; GAS-PHASE; VIBRATIONAL PREDISSOCIATION; OVERTONE SPECTROSCOPY; DISSOCIATION-ENERGY;
D O I
10.1039/c9cp03651b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An experimental benchmark data base on rotational constants, vibrational properties and energy differences for weakly and more strongly hydrogen-bonded complexes and their constituents from the spectroscopic literature is assembled. It is characterized in detail and finally contracted to a more compact, discriminatory set (ENCH-51, for Experimental Non-Covalent Harmonic with 51 entries). The meeting points between theory and experiment consist of equilibrium rotational constants and harmonic frequencies and energies, which are back-corrected from experimental observables and are very easily accessible by quantum chemical calculations. The relative performance of B3LYP-D3, PBE0-D3 and M06-2X density functional theory predictions with a quadruple-zeta basis set is used to illustrate systematic errors, error compensation and selective performance for structural, vibrational and energetical observables. The current focus is on perspectives and different benchmarking methodologies, rather than on a specific theoretical method or a specific class of compounds. Extension of the data base in chemical, observable and quantum chemical method space is encouraged.
引用
收藏
页码:18799 / 18810
页数:12
相关论文
共 36 条
  • [1] Orbital interactions in strong and weak hydrogen bonds are essential for DNA replication
    Guerra, CF
    Bickelhaupt, FM
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2002, 41 (12) : 2092 - 2095
  • [2] Interactions and applications of fuzzy, rough, and soft set in data mining
    Dash, Satya Ranjan
    Dehuri, Satchidananda
    Sahoo, Uma Kant
    International Journal of Fuzzy System Applications, 2013, 3 (03) : 37 - 50
  • [3] Aliphatic C-H•••Anion Hydrogen Bonds: Weak Contacts or Strong Interactions?
    Pedzisa, Lee
    Hay, Benjamin P.
    JOURNAL OF ORGANIC CHEMISTRY, 2009, 74 (06): : 2554 - 2560
  • [4] Less is more: how the lack of strong hydrogen bonds highlights the role of weak interactions.
    Tedesco, C.
    Pierri, G.
    Schettini, R.
    De Riccardis, F.
    Izzo, I.
    ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2022, 78 : E192 - E192
  • [5] Effects of strong hydrogen bonds and weak intermolecular interactions on supramolecular assemblies of 4-fluorobenzylamine
    Wang, Shi
    Ding, Xue-Hua
    Li, Yong-Hua
    Huang, Wei
    JOURNAL OF MOLECULAR STRUCTURE, 2015, 1091 : 98 - 108
  • [6] Azabicyclo[3.3.1]nonanone: a case when weak interactions are preferred over strong hydrogen bonds
    R. S. Rathore
    K. Sathiyanarayanan
    N. S. Karthikeyan
    P. G. Aravindan
    Structural Chemistry, 2010, 21 : 909 - 914
  • [7] Azabicyclo[3.3.1]nonanone: a case when weak interactions are preferred over strong hydrogen bonds
    Rathore, R. S.
    Sathiyanarayanan, K.
    Karthikeyan, N. S.
    Aravindan, P. G.
    STRUCTURAL CHEMISTRY, 2010, 21 (05) : 909 - 914
  • [8] STRONG HYDROGEN-BONDS IN ACID SELENITES - CORRELATION OF INFRARED SPECTROSCOPIC AND STRUCTURAL DATA
    UNTERDERWEIDE, K
    ENGELEN, B
    BOLDT, K
    JOURNAL OF MOLECULAR STRUCTURE, 1994, 322 : 233 - 239
  • [9] Iodo-nitroarenesulfonamides:: interplay of hard and soft hydrogen bonds, I•••O interactions and aromatic π•••π stacking interactions
    Kelly, CJ
    Skakle, JMS
    Wardell, JL
    Wardell, SMSV
    Low, JN
    Glidewell, C
    ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2002, 58 (58) : 94 - 108
  • [10] Soft hydrogen bonds to alkenes: the methanol-ethene prototype under experimental and theoretical scrutiny
    Heger, Matthias
    Mata, Ricardo A.
    Suhm, Martin A.
    CHEMICAL SCIENCE, 2015, 6 (07) : 3738 - 3745