相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Computational Chemistry as a Conceptual Game Changer: Understanding the Role of London Dispersion in Hexaphenylethane Derivatives (Gomberg Systems)
Soeren Roesel et al.
ISRAEL JOURNAL OF CHEMISTRY (2022)
London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey-Bakshi-Shibata Reduction
Christian Eschmann et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021)
Intramolecular London Dispersion Interactions Do Not Cancel in Solution
Jan M. Schuemann et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2021)
Could London Dispersion Force Control Regioselective (2+2) Cyclodimerizations of Benzynes? YES: Application to the Synthesis of Helical Biphenylenes
Takashi Ikawa et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2021)
Flexible C-C Bonds: Reversible Expansion, Contraction, Formation, and Scission of Extremely Elongated Single Bonds
Takuya Shimajiri et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
Longest C-C Single Bond among Neutral Hydrocarbons with a Bond Length beyond 1.8 angstrom
Yusuke Ishigaki et al.
CHEM (2018)
Probing the Delicate Balance between Pauli Repulsion and London Dispersion with Triphenylmethyl Derivatives
Soeren Roesel et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)
Sizing the role of London dispersion in the dissociation of all-meta tert-butyl hexaphenylethane
Soeren Roesel et al.
CHEMICAL SCIENCE (2017)
Distance-Dependent Attractive and Repulsive Interactions of Bulky Alkyl Groups
Jungwun Hwang et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Synthesis, Double-Helix Formation, and Higher-Assembly Formation of Chiral Polycyclic Aromatic Compounds: Conceptual Development of Polyketide Aldol Synthesis
Masahiko Yamaguchi et al.
CHEMICAL RECORD (2014)
Expandability of Ultralong C-C Bonds: Largely Different C1-C2 Bond Lengths Determined by Low-temperature X-ray Structural Analyses on Pseudopolymorphs of 1,1-Bis(4-fluorophenyl)-2,2-bis(4-methoxyphenyl)pyracene
Takanori Suzuki et al.
CHEMISTRY LETTERS (2014)
Hexaphenylethanes with an Ultra long C-C Bond: Expandability of the C-C Bond in Highly Strained Tetraarylpyracenes
Takashi Takeda et al.
CHEMISTRY LETTERS (2013)
Stable Alkanes Containing Very Long Carbon-Carbon Bonds
Andrey A. Fokin et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
Steric Crowding Can Stabilize a Labile Molecule: Solving the Hexaphenylethane Riddle
Stefan Grimme et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2011)
Synthesis of 1,8-di(1-adamantyl)naphthalenes as single enantiomers stable at ambient temperatures
Haruo Aikawa et al.
CHEMICAL COMMUNICATIONS (2011)
NCIPLOT: A Program for Plotting Noncovalent Interaction Regions
Julia Contreras-Garcia et al.
JOURNAL OF CHEMICAL THEORY AND COMPUTATION (2011)
Overcoming lability of extremely long alkane carbon-carbon bonds through dispersion forces
Peter R. Schreiner et al.
NATURE (2011)
A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu
Stefan Grimme et al.
JOURNAL OF CHEMICAL PHYSICS (2010)
Chiral Bronsted Acid-Catalyzed Allylboration of Aldehydes
Pankaj Jain et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
Strong and weak hydrogen bonds in the protein-ligand interface
Sunil K. Panigrahi et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2007)
Quantifying intermolecular interactions: Guidelines for the molecular recognition toolbox
CA Hunter
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2004)
Helical rosette nanotubes: Design, self-assembly, and characterization
H Fenniri et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2001)