-
phospholes.
Phospholes undergo different cycloaddition reactions;
coordination properties of
phospholes are also well studied. The
parent phosphole was...
-
formula C3H7P, is one atom
larger than phosphiranes, one
smaller than
phospholes, and is the heavy-atom
analogue of azetidines. The
first known phosphetane...
- J. Ashe III in 1971. Ring-opening
approaches have been
developed from
phospholes.
Structural studies by
electron diffraction reveal that
phosphorine is...
-
derivatives have
similar structure and
chemical properties to
those of
phosphole derivatives. When
arsole is
fused to a
benzene ring, this
molecule is...
- unsaturated)
Oxygen Oxolane Furan (Oxole not used)
Phosphorus Phospholane Phosphole Selenium Selenolane Selenophene Silicon Silolane Silole Sulfur Thiolane...
-
sheet (SDS)
Chemical Safety Data
Related compounds Related compounds Phosphole, arsole, bismole,
stibole Except where otherwise noted, data are given...
- an
oxygen analog Gallole, a
gallium analog Germole, a
germanium analog Phosphole, a
phosphorus analog Pyrrole (azole), a
nitrogen analog Selenophene, a...
- 1-substituted or
unsubstituted pyrrole and
related aromatic heterocyclics (
phospholes, furan, thiophene, etc.) as well as
unsubstituted or 1-substituted cyclopentadienes...
- (unsaturated: phosphirenes), five-membered
rings are
phospholanes (unsaturated:
phosphole), and six-membered
rings are phosphinanes.
Tertiary (3°) phosphines, with...
- The
phosphole component has been
shown by Reau et al. in 2002 to be
prone to hyperpolarizability. This
characteristic is more true of
phospholes when...
