Visible light radical photoinitiators of polymerization based on photochromic molecules
Dyes and Pigments,
Journal Year:
2024,
Volume and Issue:
226, P. 112139 - 112139
Published: April 4, 2024
Language: Английский
Combined Photopolymerization and Localized Photochromism Generation by Aza-Diarylethene and Hemiindigo Synergy
Maximilian Sacherer,
No information about this author
Henry Dube
No information about this author
Published: Aug. 1, 2024
Molecular
photoswitches
produce
light-controlled
changes
at
the
nanometer
scale
and
can
therefore
be
used
to
alter
states
behavior
of
materials
in
a
truly
bottom-up
fashion.
Here
we
show
an
escalating
photonic
complexity
material
property
control
with
light
using
recently
developed
aza-diarylethene
combination
hemiindigo
(HI)
photoswitches.
First,
as
photoswitch
polystyrene
(PS)
inscribe
relief-type
3D
structures
reversibly
into
PS.
Second,
aza-
diarylethene
further
photoinitiator
for
light-induced
polymerization
acrylates,
demonstrating
first
time
chemical
reactivity
its
zwitterionic
switching
state.
Third,
HIs
are
implemented
polymerized
PMA,
generating
photochromic
polymers.
At
fourth
level,
binary
mixture
allows
synergize
induced
photopolymerization
localized
photochromism
simultaneously
entrapped
functional
HI.
With
such
multi-level
response,
utility
this
particular
applications
advanced
is
demonstrated.
Language: Английский
Methods for functionalization of anthraquinones
Russian Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
93(10), P. RCR5141 - RCR5141
Published: Oct. 1, 2024
Language: Английский
Combined Photopolymerization and Localized Photochromism by Aza‐Diarylethene and Hemiindigo Synergy
Maximilian Sacherer,
No information about this author
Henry Dube
No information about this author
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 21, 2024
Abstract
Molecular
photoswitches
produce
light‐controlled
changes
at
the
nanometer
scale
and
can
therefore
be
used
to
alter
states
behavior
of
materials
in
a
truly
bottom‐up
fashion.
Here
an
escalating
photonic
complexity
material
property
control
with
light
is
shown
using
recently
developed
aza‐diarylethene
combination
hemiindigo
(HI)
photoswitches.
First,
as
photoswitch
polystyrene
(PS)
reversibly
inscribe
relief‐type
3D
structures
into
PS.
Second,
further
photoinitiator
for
light‐induced
polymerization
methyl
acrylate
(MA),
demonstrating
first
time
chemical
reactivity
its
zwitterionic
switching
state.
Third,
HIs
are
implemented
polymerized
MA,
generating
photochromic
polymers.
At
fourth
level,
binary
mixture
allows
synergize
aza‐diarylethene‐induced
photopolymerization
localized
photochromism
simultaneously
entrapped
functional
HI.
With
such
multilevel
response,
utility
this
particular
applications
advanced
demonstrated.
Language: Английский
Second Generation Zwitterionic Aza‐Diarylethene: Photoreversible CN Bond Formation, Three‐State Photoswitching, Thermal Energy Release, and Facile Photoinitiation of Polymerization
Henry Dube,
No information about this author
Maximilian Sacherer
No information about this author
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 21, 2024
Abstract
Diarylethenes
are
a
well‐studied
and
optimized
class
of
photoswitches
with
wide
range
applications,
including
data
storage,
smart
materials,
or
photocontrolled
catalysis
biological
processes.
Most
recently,
aza‐diarylethenes
have
been
developed
in
which
carbon‐carbon
bond
connections
replaced
by
carbon‐nitrogen
connections.
This
structural
elaboration
opens
up
an
entire
new
structure
property
space
expanding
the
versatility
applicability
diarylethenes.
In
this
work,
we
present
second
generation
zwitterionic
aza‐diarylethenes,
finally
allows
for
fully
reversible
photoswitching
precise
control
over
all
three
switching
states.
High‐yielding
between
neutral
open
form
Z
isomer
is
achieved
two
different
wavelengths
light.
The
third
E
isomeric
state
can
be
reached
to
87
%
upon
irradiation
wavelength.
Its
high
energy
content
>10
kcal/mol
released
thermally
deliberate
solvent
change
as
trigger
mechanism,
rendering
into
interesting
candidates
molecular
solar
thermal
storage
(MOST)
applications.
also
serves
locking
state,
allowing
toggle
light‐responsiveness
reversibly
labile
stable
switching.
Further,
states
leads
highly
efficient
photopolymerization
methyl
acrylate
(MA),
directly
harnessing
unleashed
chemical
reactivity
our
aza‐diarylethene
materials
application.
Language: Английский
Second Generation Zwitterionic Aza‐Diarylethene: Photoreversible CN Bond Formation, Three‐State Photoswitching, Thermal Energy Release, and Facile Photoinitiation of Polymerization
Henry Dube,
No information about this author
Maximilian Sacherer
No information about this author
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 21, 2024
Abstract
Diarylethenes
are
a
well‐studied
and
optimized
class
of
photoswitches
with
wide
range
applications,
including
data
storage,
smart
materials,
or
photocontrolled
catalysis
biological
processes.
Most
recently,
aza‐diarylethenes
have
been
developed
in
which
carbon‐carbon
bond
connections
replaced
by
carbon‐nitrogen
connections.
This
structural
elaboration
opens
up
an
entire
new
structure
property
space
expanding
the
versatility
applicability
diarylethenes.
In
this
work,
we
present
second
generation
zwitterionic
aza‐diarylethenes,
finally
allows
for
fully
reversible
photoswitching
precise
control
over
all
three
switching
states.
High‐yielding
between
neutral
open
form
Z
isomer
is
achieved
two
different
wavelengths
light.
The
third
E
isomeric
state
can
be
reached
to
87
%
upon
irradiation
wavelength.
Its
high
energy
content
>10
kcal/mol
released
thermally
deliberate
solvent
change
as
trigger
mechanism,
rendering
into
interesting
candidates
molecular
solar
thermal
storage
(MOST)
applications.
also
serves
locking
state,
allowing
toggle
light‐responsiveness
reversibly
labile
stable
switching.
Further,
states
leads
highly
efficient
photopolymerization
methyl
acrylate
(MA),
directly
harnessing
unleashed
chemical
reactivity
our
aza‐diarylethene
materials
application.
Language: Английский
All-Visible-Light-Activated Diarylethene Photoswitches
Ruiji Li,
No information about this author
Ting Ou,
No information about this author
Wen Li
No information about this author
et al.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(21), P. 5202 - 5202
Published: Nov. 3, 2024
Photochromic
compounds
have
attracted
much
attention
for
their
potential
applications
in
photo-actuators,
optoelectronic
devices
and
optical
recording
techniques.
This
interest
is
driven
by
key
photochemical
photophysical
properties,
which
can
be
reversibly
modulated
light
irradiation.
Among
them,
diarylethene
garnered
extensive
investigation
due
to
excellent
thermal
stability
of
both
open-
closed-form
isomers,
robust
fatigue
resistance,
high
photocyclization
quantum
yield
good
photochromic
performance
solution
solid
phases.
However,
a
notable
limitation
expanding
the
utility
necessity
ultraviolet
induce
photochromism.
requirement
poses
challenges,
as
detrimental
biological
tissues,
its
penetration
often
restricted
various
media.
review
provides
an
overview
design
strategies
employed
development
visible-light-responsive
compounds.
These
serve
guideline
molecular
design,
with
significantly
broaden
all-visible-light-activated
realms
materials
science
biomedical
science.
Language: Английский