TY - JOUR
T1 - Helium Accepts Back-Donation in Highly Polar Complexes
T2 - New Insights into the Weak Chemical Bond
AU - Nunzi, Francesca
AU - Cesario, Diego
AU - Pirani, Fernando
AU - Belpassi, Leonardo
AU - Frenking, Gernot
AU - Grandinetti, Felice
AU - Tarantelli, Francesco
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/7/20
Y1 - 2017/7/20
N2 - We studied the puzzling stability and short distances predicted by theory for helium adducts with some highly polar molecules, such as BeO or AuF. On the basis of high-level quantum-chemical calculations, we carried out a detailed analysis of the charge displacement occurring upon adduct formation. For the first time we have unambiguously ascertained that helium is able not only to donate electron density, but also, unexpectedly, to accept electron density in the formation of weakly bound adducts with highly polar substrates. The presence of a large dipole moment induces a large electric field at He, which lowers its 2p orbital energy and enables receipt of π electron density. These findings offer unprecedented important clues toward the design and synthesis of stable helium compounds.
AB - We studied the puzzling stability and short distances predicted by theory for helium adducts with some highly polar molecules, such as BeO or AuF. On the basis of high-level quantum-chemical calculations, we carried out a detailed analysis of the charge displacement occurring upon adduct formation. For the first time we have unambiguously ascertained that helium is able not only to donate electron density, but also, unexpectedly, to accept electron density in the formation of weakly bound adducts with highly polar substrates. The presence of a large dipole moment induces a large electric field at He, which lowers its 2p orbital energy and enables receipt of π electron density. These findings offer unprecedented important clues toward the design and synthesis of stable helium compounds.
UR - http://www.scopus.com/inward/record.url?scp=85025161192&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.7b01320
DO - 10.1021/acs.jpclett.7b01320
M3 - 文章
C2 - 28636399
AN - SCOPUS:85025161192
SN - 1948-7185
VL - 8
SP - 3334
EP - 3340
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 14
ER -