-
Diimide, also
called diazene or diimine, is a
compound having the
formula HN=NH. It
exists as two
geometric isomers, E (trans) and Z (cis). The term diazene...
- 60 °C to give the
diimide. However, most
sulfur diimides are not
produced from such
elimination reactions. Typically,
sulfur diimides arise from treatment...
- into, once again, two subclasses:
Perylene Diimides (PDIs) and
Naphthalene Diimides (NDIs).
Rylene diimides consist of a
planar rylene framework and numerous...
-
Reductions with
diimide are a
chemical reactions that
convert unsaturated organic compounds to
reduced alkane products. In the process,
diimide (N 2H 2) is...
- Jani,
Chintan H.; Langford,
Steven J. (2008). "Chemistry of
naphthalene diimides". Chem. Soc. Rev. 37 (2): 331–342. doi:10.1039/b615857a. PMID 18197349...
- the
diimide derivatives of perylene-3,4:9,10-tetracarboxylic
dianhydride and terrylene-3,4:11,12-tetracarboxylic dianhydride.
Naphthalene diimides (NDIs)...
-
least conjugated double bond,
showcasing the
precision of
reductions with
diimides in
targeted organic synthesis.
Group transfer reactions are
prevalent in...
- Barlow, S., Marder, S. (2011), Perylene-3,4,9,10-tetracarboxylic Acid
Diimides: Synthesis,
Physical Properties, and Use in
Organic Electronics. Journal...
- The N≡C–NH2 form dominates, but in a few
reactions (e.g. silylation) the
diimide form
appears to be important.
Cyanamide dimerizes to give 2-cyanoguanidine...
-
structure F−N=N−F and
exists in both cis and
trans isomers, as
typical for
diimides. The cis
isomer has C2v
symmetry and the
trans isomer has C2h symmetry...
