bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 22, 2024
Abstract
Current
challenges
in
tissue
engineering
include
creation
of
extracellular
environments
that
support
and
interact
with
cells
using
biochemical,
mechanical,
structural
cues.
Spatial
control
over
these
cues
is
currently
limited
due
to
a
lack
suitable
fabrication
techniques.
This
study
introduces
Xolography,
an
emerging
dual-color
light-sheet
volumetric
printing
technology,
achieve
mechanical
features
for
hydrogel-based
photoresins
at
micro-to
macroscale
while
within
minutes.
We
propose
water-soluble
photoswitch
photoinitiator
system
are
the
first
demonstrate
Xolography
library
naturally-derived,
synthetic,
thermoresponsive
hydrogels.
Centimeter-scale,
three-dimensional
constructs
positive
20
µm
negative
∼
100
fabricated
properties
(compressive
moduli
0.2
kPa
–
6.5
MPa).
Notably,
switching
from
binary
grayscaled
light
projection
enables
spatial
stiffness
(0.2
16
kPa).
As
proof
concept,
leveraged
hydrogels
introduce
reversible
anisotropic
shape
changes
beyond
isometric
shrinkage.
finally
viable
cell
aggregates,
laying
foundation
cell-laden
dynamic,
cell-instructive
tunable
fast
one-step
process.
Overall,
innovations
unlock
unique
possibilities
across
multiple
biomedical
applications.
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.
Nachrichten aus der Chemie,
Journal Year:
2024,
Volume and Issue:
72(10), P. 52 - 59
Published: Sept. 30, 2024
Abstract
Responsive
Polymere
ändern
ihre
Materialeigenschaften
und
reagieren
über
programmierte
molekulare
Prozesse
auf
Umwelteinflüsse.
Solche
Materialdesigns
standen
dieses
Jahr
im
Fokus
vieler
Anwendungen:
Sie
verbessern
die
Rezyklierbarkeit,
führen
zu
selbstreguliertem
Abbau
Selbstheilung,
transportieren
Wirkstoffe
setzen
sie
frei
oder
ahmen
biologische
Systeme
mit
komplexen
Signalverarbeitungsabläufen
adaptiven
Strukturen
nach.
Für
eine
nachhaltige
Kunststoffwirtschaft
bleiben
zudem
leitfähige
biobasierte
Monomere
wichtig.
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.
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.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 22, 2024
Abstract
Current
challenges
in
tissue
engineering
include
creation
of
extracellular
environments
that
support
and
interact
with
cells
using
biochemical,
mechanical,
structural
cues.
Spatial
control
over
these
cues
is
currently
limited
due
to
a
lack
suitable
fabrication
techniques.
This
study
introduces
Xolography,
an
emerging
dual-color
light-sheet
volumetric
printing
technology,
achieve
mechanical
features
for
hydrogel-based
photoresins
at
micro-to
macroscale
while
within
minutes.
We
propose
water-soluble
photoswitch
photoinitiator
system
are
the
first
demonstrate
Xolography
library
naturally-derived,
synthetic,
thermoresponsive
hydrogels.
Centimeter-scale,
three-dimensional
constructs
positive
20
µm
negative
∼
100
fabricated
properties
(compressive
moduli
0.2
kPa
–
6.5
MPa).
Notably,
switching
from
binary
grayscaled
light
projection
enables
spatial
stiffness
(0.2
16
kPa).
As
proof
concept,
leveraged
hydrogels
introduce
reversible
anisotropic
shape
changes
beyond
isometric
shrinkage.
finally
viable
cell
aggregates,
laying
foundation
cell-laden
dynamic,
cell-instructive
tunable
fast
one-step
process.
Overall,
innovations
unlock
unique
possibilities
across
multiple
biomedical
applications.