1,4-Dihydropyrrolo[3,2-b]Pyrroles Containing New A-D-A System: Synthesis and Investigation of Their Photophysical Properties
Journal of Fluorescence,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 21, 2025
Abstract
Herein,
new
tetraarylpyrrolo[3,2-b]pyrroles
(TAPP)
containing
different
substituents
(
4a-c
,
5a-c
)
on
the
N
-phenyl
rings
were
synthesized
in
high
yields
using
a
one-pot
method.
The
3,6
positions
of
pyrrolopyrol
ring
compound
formylated
by
Vilsmeier-Haack
reaction
to
synthesize
acceptor-donor-acceptor
(A-D-A)
system
).
photophysical
properties
all
obtained
derivatives
investigated
solvents.
According
results
obtained,
absorptions
recorded
around
400
nm
and
their
emission
intensities
appeared
450
nm.
absorption
4b
5b
as
350
nm,
respectively,
while
observed
455
440.
In
A-D-A
formed
result
bonding
electron-withdrawing
formyl
groups
at
position
TAPP
structure,
Stokes
shift
occurred,
50
hypsochromic
shifts
its
absorption.
Language: Английский
Diversifying peripheral aromatic units of pyrrolo[3,2-b]pyrrole-containing conjugated polymers and the resulting optoelectronic properties
Graham S. Collier,
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Julien T. Layton,
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Perry Skiouris
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et al.
Journal of Materials Chemistry C,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Pyrrolo[3,2-
b
]pyrrole
represents
a
synthetically-simple
conjugated
scaffold
that
enables
accessing
polymers
with
tailorable
properties
useful
for
organic
electronics.
Language: Английский