The CH/p interaction 1,† is the weakest extreme of hydrogen bonds 2, 3 that occurs between a soft acid (CH) and a soft base (p-system) 4, 5 in the context of Pearson's HSAB principle …
The nature and characteristics of the CH/π interaction are discussed by comparison with other weak molecular forces such as the CH/O and OH/π interaction. The CH/π interaction is …
M Nishio, Y Umezawa, K Honda, S Tsuboyama… - …, 2009 - pubs.rsc.org
This treatise is an update to a preceding highlight (CH/π hydrogen bonds in crystals) published in this journal 5 years ago (M. Nishio, CrystEngComm, 2004, 6, 130–156). After …
The two-volume Encyclopedia of Supramolecular Chemistry offers authoritative, centralized information on a rapidly expanding interdisciplinary field. User-friendly and high-quality …
I Sandler, J Chen, M Taylor, S Sharma… - The Journal of Physical …, 2021 - ACS Publications
The DLPNO-CCSD (T) method is designed to study large molecular systems at significantly reduced cost relative to its canonical counterpart. However, the error in this approach is also …
K Shibasaki, A Fujii, N Mikami… - The Journal of Physical …, 2006 - ACS Publications
The accurate CH/π interaction energy of the benzene− methane model system was experimentally and theoretically determined. In the experiment, mass analyzed threshold …
LR Domingo, J Andrés - The Journal of Organic Chemistry, 2003 - ACS Publications
To examine how hydrogen-bond (HB) formation involving chloroform solvent molecules influences the chemical reactivity of ketones, the hetero-Diels− Alder reaction of N, N …
X Zhang, H Du, Z Wang, YD Wu… - The Journal of Organic …, 2006 - ACS Publications
The enantioselective hetero-Diels− Alder (HDA) reaction of Danishefsky's diene with benzaldehyde has been achieved catalytically by a series of α, α, α ', α '-tetraaryl-1, 3 …
A catalytic asymmetric hetero-Diels–Alder (HDA) reaction has been achieved through hydrogen-bond directed γ-addition of olefinic azlactones to isatins. This methodology …