Polymer Chemistry,
Journal Year:
2023,
Volume and Issue:
15(4), P. 321 - 331
Published: Dec. 16, 2023
Herein,
we
exploit
chemical
amplification
to
release
–OH
groups
in
dynamic
covalent
photopolymers
on-demand.
Via
a
single
photon
event,
cascade
of
reactions
occurs,
which
allows
the
polymers
flow
through
thermo-activated
transesterification.
European Polymer Journal,
Journal Year:
2024,
Volume and Issue:
205, P. 112718 - 112718
Published: Jan. 2, 2024
In
the
contemporary
era,
novel
manufacturing
technologies
like
additive
(AM)
have
revolutionized
different
engineering
sectors
including
biomedical,
aerospace,
electronics,
etc.
Four-dimensional
(4D)
printing
aka
AM
of
smart
materials
is
gaining
popularity
among
scientific
community,
which
has
excellent
ability
to
make
soft
structures
such
as
robots,
actuators,
and
grippers.
These
are
developed
by
applying
various
stimuli
pH,
temperature,
magnetic
field,
many
combinations
onto
materials.
Stimuli
in
3D
permit
shape-morphing
behaviors
bending,
twisting,
folding,
swelling,
rolling,
shrinking,
origami,
or
locomotion.
A
wide
variety
can
be
fabricated
through
incorporation
hard
particles
into
resulting
magneto-active
(MASMs).
With
this
integration,
magneto-thermal
coupling
actuation
allows
diverse
magneto-deformations,
facilitating
development
personalized
devices
that
capable
enhanced
deformation.
review,
guidelines
provided
on
for
MASMs
polymers
(MAPs),
composites,
hydrogels
(MAHs)
booming
flexible
wearable
biomimetic
devices.
Moreover,
3D-printed
robotics
an
outstanding
capacity
adapt
complicated
situations
advanced
actuating
applications.
Finally,
some
current
challenges
emerging
areas
exciting
technology
been
proposed.
Lastly,
it
anticipated
technological
advancements
developing
intelligent
will
a
significant
impact
design
real-world
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 29, 2024
Abstract
Epoxy
resins‐based
engineering
plastics
are
indispensable
in
the
global
economy,
but
they
have
created
a
serious
waste
crisis
caused
by
their
chemical
cross‐linked
networks.
To
solve
this
problem,
current
strategies
often
require
assistance
of
catalysts
or
solvents
at
expense
thermal
and
mechanical
performance.
In
work,
high‐performance
epoxy
resin
featuring
dynamic
ester
disulfide
bonds
(TDS)
is
reported,
which
exhibits
higher
properties
than
common
plastics,
i.e.,
tensile
strength
modulus
66.6
MPa
2.63
GPa,
flexural
103.2
3.52
glass
transition
temperature
(
T
g
)
133
°C.
Moreover,
reversible
transformation
between
aromatic
thiyl
radicals
endows
TDS
with
autonomous
visualization
damage
healing.
addition,
harmonious
interplay
bonds‐promoted
tertiary
amine
accelerated
topological
network
rearrangements,
enabling
to
easily
reshape
weld.
Specifically,
can
be
completely
degraded
pure
water
200
°C
without
any
catalyst,
products
directly
re‐polymerized
achieve
green
closed‐loop
recycling.
This
work
proposes
simple
economical
strategy
for
development
resin‐based
cutting‐edge
that
both
functional
sustainable.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(20)
Published: March 16, 2024
Vitrimers
represent
an
emerging
class
of
polymeric
materials
that
combine
the
desirable
characteristics
both
thermoplastics
and
thermosets
achieved
through
design
dynamic
covalent
bonds
within
polymer
networks.
However,
these
are
prone
to
creep
due
inherent
instability
bonds.
Consequently,
there
pressing
demands
for
development
robust
stable
chemistries.
Here,
we
report
a
catalyst-free
α-acetyl
cinnamate/acetoacetate
(α-AC/A)
exchange
reaction
develop
vitrimers
with
remarkable
resistance.
Small-molecule
model
studies
revealed
α-AC/A
occurred
at
temperatures
above
140
°C
in
bulk,
whereas
120
°C,
this
was
absent.
For
demonstration
case
polymers,
copolymers
derived
from
common
vinyl
monomers
were
crosslinked
terephthalaldehyde
produce
tunable
thermal
mechanical
performance.
All
resulting
exhibited
high
stability,
especially
terms
resistance
while
retaining
commendable
reprocessability
when
subjected
temperatures.
This
work
showcases
as
novel
chemistry
capable
imparting
stability
cross-linked
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(19), P. 13367 - 13376
Published: May 2, 2024
The
use
of
internal
catalysts
has
emerged
as
a
pivotal
design
principle
to
facilitate
dynamic
exchanges
within
covalent
adaptable
networks
(CANs).
Polybenzoxazines,
specifically,
have
shown
considerable
potential
in
generating
vitrimers
through
thermally
induced
transesterification
reactions
catalyzed
internally
by
tertiary
amines.
This
study
aims
investigate
the
chemical
complexities
benzoxazine
vitrimers.
To
achieve
this,
model
molecules
using
various
phenolic
acids
and
amino-alcohol
derivatives
were
synthesized
precursors.
structure
these
was
fully
elucidated
nuclear
magnetic
resonance
(NMR).
Differential
scanning
calorimetry
(DSC)
rheology
experiments
evidenced
accelerated
network
formation
precursors
due
presence
aliphatic
−OH
groups.
Thermogravimetric
analysis
coupled
with
microcomputed
gas
chromatography
(TGA-μGC)
used
provide
evidence
reactions.
results
showed
that
spatial
proximity
between
amine
hydroxyl
groups
significantly
enhances
rate
exchange,
attributed
neighboring
group
participation
(NGP)
effect.
Interestingly,
kinetic
complementary
NMR
techniques
revealed
thermal
latency
toward
its
opening
is
needed
trigger
exchange.
highlights
crucial
role
steric
hindrance
basicity
promoting
exchange
an
system.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(21)
Published: April 5, 2024
Abstract
Dynamically
crosslinked
polymers
(DCPs)
have
gained
significant
attention
owing
to
their
applications
in
fabricating
(re)processable,
recyclable,
and
self‐healable
thermosets,
which
hold
great
promise
addressing
ecological
issues,
such
as
plastic
pollution
resource
scarcity.
However,
the
current
research
predominantly
focuses
on
redefining
and/or
manipulating
geometries
while
replicating
bulk
properties.
Given
inherent
design
flexibility
of
dynamic
covalent
networks,
DCPs
also
exhibit
a
remarkable
potential
for
various
novel
through
postsynthesis
reprogramming
In
this
review,
recent
advancements
strategies
that
enable
transform
properties
after
synthesis
are
presented.
The
underlying
mechanisms
associated
material
overviewed
mainly
three
distinct
strategies,
namely
latent
catalysts,
material‐growth,
topology
isomerizable
networks.
Furthermore,
mutual
relationship
impact
these
when
integrated
within
one
system
discussed.
Finally,
application
prospects
relevant
issues
necessitating
further
investigation,
along
with
solutions
analyzed.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
34(2)
Published: Sept. 28, 2023
Abstract
The
utilization
of
dynamic
cross‐linking
represents
a
highly
promising
approach
in
addressing
the
escalating
issues
plastic
pollution
and
fossil
resource
consumption.
Despite
being
extensively
investigated
over
past
decade,
various
dynamically
cross‐linked
polymers
(DCPs)
predominantly
remain
confined
to
realm
academic
research.
To
serve
as
valuable
material
for
practical
application,
advanced
processing
is
always
essential
all
kinds
materials.
3D
printing
(3DP)
enables
creation
intricate
shapes
layer‐by‐layer
without
relying
on
molds,
thus
integration
3DP
techniques
with
DCPs
holds
significant
potential
enhance
expand
applicability
DCPs.
Here,
an
overview
fundamental
principles
underlying
compatible
are
provided,
namely
photocuring
3DP,
extrusion‐based
laser
sintering‐based
3DP.
Additionally,
comprehensive
summary
representative
research
works
that
specifically
focus
application
each
respective
technique
presented.
performance
mechanism
involved
corresponding
process
thoroughly
discussed
comprehensively
reviewed.
Finally,
existing
challenges
pertaining
further
enhancing
printability,
performance,
efficiency,
etc.,
deliberated
upon,
while
proposing
directions
address
these
concerns.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 3, 2024
Supramolecular
adhesion
material
systems
based
on
small
molecules
have
shown
great
potential
to
unite
the
contradiction
between
strong
and
reversibility.
However,
these
suffer
from
low
strength/narrow
span,
limited
designability,
single
interaction
due
fewer
covalent
bond
content
action
sites
in
molecules.
Herein,
an
ultrahigh-strength
large-span
reversible
adhesive
enabled
by
a
branched
oligomer
controllable
self-aggregation
strategy
is
developed.
The
dense
bonds
present
oligomers
greatly
enhance
strength
without
compromising
resulting
exhibits
of
≈140
times,
switching
ultra-strong
tough
(5.58
MPa
5093.92
N
m
ACS Macro Letters,
Journal Year:
2023,
Volume and Issue:
12(11), P. 1536 - 1542
Published: Nov. 1, 2023
The
industrial
implementation
of
covalent
adaptable
networks
hinges
on
the
delicate
task
achieving
rapid
bond
exchange
activation
at
specific
temperatures
while
ensuring
a
sufficiently
slow
working
to
avoid
irreversible
deformation.
In
this
pursuit,
latent
catalysts
offer
potential
solution,
allowing
for
spatiotemporal
control
dynamic
in
vitrimer
networks.
However,
nature
their
has
led
undesired
creep
deformation
after
multiple
cycles
reprocessing.
work,
we
demonstrate
that
tetraphenylborate
tetramethyl
guanidinium
salt
(TPB:TMG)
undergoes
reversible
thermal
dissociation,
releasing
free
TMG.
This
thermally
organocatalyst
can
be
readily
introduced
as
an
additive
industrially
relevant
materials
such
disulfide-containing
polyurethane
(PU)
undergo
disulfide
presence
base
catalyst.
contrast
with
free-base-catalyzed
process,
dual
benefit
adding
TPB:TMG
preventing
lower
and
also
enabling
reprocessability
PU
elevated
temperatures.
remarkable
reversibility
activated
catalyst
allows
reprocessing
effectively
maintaining
creep-free
state
service
temperature.