"Hydridic Hydrogen-Bond Donors" Are Not Hydrogen-Bond Donors

被引:2
作者
Santos, Lucas de Azevedo [1 ]
Vermeeren, Pascal [1 ]
Bickelhaupt, F. Matthias [1 ,2 ,3 ]
Guerra, Celia Fonseca [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Chem & Pharmaceut Sci, AIMMS, NL-1081 HZ Amsterdam, Netherlands
[2] Radboud Univ Nijmegen, Inst Mol & Mat, NL-6525 AJ Nijmegen, Netherlands
[3] Univ Johannesburg, Dept Chem Sci, ZA-2006 Johannesburg, South Africa
关键词
CHEMISTRY;
D O I
10.1021/jacs.4c07821
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we dismiss a recent proposal by Civis, Hobza, and co-workers to modify the IUPAC definition of hydrogen bonds in order to expand the scope from protonic Y-H delta+ to hydridic Y-H(delta- )hydrogen-bond donor fragments [J. Am. Chem. Soc. 2023, 145, 8550]. Based on accurate Kohn-Sham molecular orbital (KS-MO) analyses, we falsify the conclusion that interactions involving protonic and hydridic hydrogens are both hydrogen bonds; they are not. Instead, our quantitative KS-MO, energy decomposition, and Voronoi deformation density analyses reveal two fundamentally different bonding mechanisms for protonic Y-H delta+ and hydridic Y-H delta- fragments which go with charge transfer in opposite directions. On one hand, we confirm the IUPAC definition for regular hydrogen bonds in the case of protonic Y-H delta+ fragments. On the other hand, complexes involving Y-H delta- fragments are, in fact, acceptors in other well-known families of Lewis-acid/base interactions, such as halogen bonds, chalcogen bonds, and pnictogen bonds. These mechanisms lead to the same spectroscopic phenomenon in both the Y-H delta+ and Y-H delta- fragments, that is, the redshift in the Y-H stretching frequency, which is, thus, not an exclusive indicator for hydrogen bonding.
引用
收藏
页码:25701 / 25709
页数:9
相关论文
共 50 条
  • [31] A Triazine Based Porous Organic Polymer as an Efficient Hydrogen-Bond Donor and Acceptor Cooperative Heterogeneous Catalyst for the Synthesis of 2-Substituted Benzimidazoles
    Vijayan, Aswathy Panalukudiyil
    Pallikkara, Athira
    Ramakrishnan, Kala
    Kumar, Rakesh S.
    Jayasree, Elambalassery G.
    CHEMISTRYSELECT, 2023, 8 (42):
  • [32] Hydrogen bond and halogen bond inside the carbon nanotube
    Wang, Weizhou
    Wang, Donglai
    Zhang, Yu
    Ji, Baoming
    Tian, Anmin
    JOURNAL OF CHEMICAL PHYSICS, 2011, 134 (05)
  • [33] Self-Assembly of a Two-Dimensional Bimetallic Coordination Framework and Dynamic Control of Reversible Conversions to Homo-Metallic Hydrogen-Bond Arrays
    Shi, Ziliang
    Lin, Nian
    CHEMPHYSCHEM, 2010, 11 (01) : 97 - 100
  • [34] Metal-Templated Hydrogen Bond Donors as "Organocatalysts" for Carbon-Carbon Bond Forming Reactions: Syntheses, Structures, and Reactivities of 2-Guanidinobenzimidazole Cyclopentadienyl Ruthenium Complexes
    Scherer, Alexander
    Mukherjee, Tathagata
    Hampel, Frank
    Gladysz, John A.
    ORGANOMETALLICS, 2014, 33 (23) : 6709 - 6722
  • [35] Hexaamminecobalt(III) Cation as Multiple Hydrogen Bond Donors: Synthesis, Characterization and Energetic Properties of cyclo- Pentazolate and Azide Based Complexes
    Xu, Yuangang
    Zhou, Jianxin
    Li, Dongxue
    Wang, Pengcheng
    Lin, Qiuhan
    Lu, Ming
    CRYSTAL GROWTH & DESIGN, 2023, 23 (02) : 811 - 819
  • [36] Iodine(III)-Based Halogen Bond Donors: Properties and Applications
    Robidas, Raphael
    Reinhard, Dominik L.
    Legault, Claude Y.
    Huber, Stefan M.
    CHEMICAL RECORD, 2021, 21 (08) : 1912 - 1927
  • [37] Organic fluorines as halogen bond donors: Theoretical study and crystallographic evidence
    Wang, Yanhua
    Tong, Jianying
    Wu, Weihong
    Xu, Zhijian
    Lu, Yunxiang
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2015, 115 (14) : 884 - 890
  • [38] Use of Hydrogen Donors for Partial Upgrading of Heavy Petroleum
    Aleman-Vazquez, Laura O.
    Torres-Mancera, Pablo
    Ancheyta, Jorge
    Ramirez-Salgado, Joel
    ENERGY & FUELS, 2016, 30 (11) : 9050 - 9060
  • [39] Activatable Small-Molecule Hydrogen Sulfide Donors
    Levinn, Carolyn M.
    Cerda, Matthew M.
    Pluth, Michael D.
    ANTIOXIDANTS & REDOX SIGNALING, 2020, 32 (02) : 96 - 109
  • [40] A highly hydrated α-cyclodextrin/1-undecanol inclusion complex: crystal structure and hydrogen-bond network from high-resolution neutron diffraction at 20K
    Gallois-Montbrun, Delphine
    Le Bas, Genevieve
    Mason, Sax A.
    Prange, Thierry
    Lesieur, Sylviane
    ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2013, 69 : 214 - 227