Polymer Chemistry,
Journal Year:
2018,
Volume and Issue:
9(33), P. 4332 - 4342
Published: Jan. 1, 2018
Phenylhydrazine
is
an
effective
modifier
for
conventional
ATRP
syntheses,
providing
systematic
control
over
the
dispersity
of
polymers
with
unimodal
molecular
weight
distributions.
Chemical Science,
Journal Year:
2022,
Volume and Issue:
13(22), P. 6541 - 6549
Published: Jan. 1, 2022
Along-wavelength
emissive
Ru(
ii
)
metallacycle
chemo-phototheranostic
was
prepared
via
self-assembly
that
exhibits
excellent
photostability,
deep-tissue
penetration
capability,
and
promising
chemo-phototherapeutic
performance
in
vitro
vivo
.
Angewandte Chemie International Edition,
Journal Year:
2021,
Volume and Issue:
60(35), P. 19383 - 19388
Published: June 16, 2021
The
breadth
and
the
shape
of
molecular
weight
distributions
can
significantly
influence
fundamental
polymer
properties
that
are
critical
for
various
applications.
However,
current
approaches
require
extensive
synthesis
multiple
polymers,
limited
in
dispersity
precision
typically
incapable
simultaneously
controlling
both
distributions.
Here
we
report
a
simplified
approach,
whereby
on
mixing
two
polymers
(one
high
Đ
one
low
Đ),
any
intermediate
value
be
obtained
(e.g.
from
1.08
to
1.84).
Unrivalled
is
achieved,
with
values
even
nearest
0.01
1.37→1.38→1.39→1.40→1.41→1.42→1.43→1.44→1.45),
while
maintaining
fairly
monomodal
This
approach
was
also
employed
control
obtain
diblock
copolymers
accuracy.
straightforward
nature
our
methodology
alongside
its
compatibility
wide
range
polymerisation
protocols
ATRP,
RAFT),
expands
toolbox
tailored
polymeric
materials
makes
them
accessible
all
researchers.
Angewandte Chemie International Edition,
Journal Year:
2019,
Volume and Issue:
58(17), P. 5598 - 5603
Published: Feb. 20, 2019
Molecular
weight
distribution
of
polymers,
termed
dispersity
(Đ),
is
a
fundamental
parameter
for
determining
polymer
material
properties.
This
paper
reports
novel
approach
controlling
Đ
by
exploiting
temperature-selective
radical
generation
in
organocatalyzed
living
polymerization.
The
polymers
with
tailored
were
synthesized
batch
system
without
the
assistance
an
external
pump.
A
unique
aspect
this
that
was
tuneable
from
1.11
to
1.50
any
segment
diblock,
triblock,
and
multiblock
copolymers
form
star
brush
segmental
or
topological
restriction.
amenable
various
monomers
free
metals
thus
attractive
applications.
also
generated
brushes
on
surfaces
Đ.
An
interesting
finding
exhibited
interaction
molecules,
depending
value.
ACS Macro Letters,
Journal Year:
2018,
Volume and Issue:
7(6), P. 677 - 682
Published: May 24, 2018
The
molecular
weight
distributions
(MWDs)
of
block
copolymers
significantly
impact
their
morphological
phase
behavior,
but
exploiting
these
features
as
a
means
to
tune
material
properties
has
been
limited
the
MWD
breadth,
or
dispersity
(Đ).
Manipulation
entire
promising
potential
address
this
challenge
by
providing
convenient
and
versatile
route
toward
tailoring
polymer
nanostructure.
Herein,
we
describe
self-assembly
poly(styrene)-block-poly(2-vinylpyridine)
(PS-b-P2VP)
where
PS
blocks
have
systematically
deviating
compositions
weights.
We
find
that
controlling
shape,
breadth
skew,
afforded
access
different
morphologies
in
samples
with
same
characteristics,
including
Đ.
As
such,
illustrate
generality
effectiveness
strategy
anticipate
it
will
facilitate
increased
deployment
disperse
advanced
materials
applications.
Polymer Chemistry,
Journal Year:
2020,
Volume and Issue:
11(35), P. 5559 - 5571
Published: Jan. 1, 2020
The
development
and
applications
of
an
organocatalyzed
living
radical
polymerization
via
halogen-bonding
catalysis,
i.e.,
reversible
complexation
mediated
(RCMP),
are
highlighted.
Polymer Chemistry,
Journal Year:
2019,
Volume and Issue:
11(2), P. 326 - 336
Published: June 13, 2019
Polymer
molecular
weight
distributions
are
targeted
through
kinetic
modeled
with
high
fidelity
based
on
the
temporal
control
of
chain
initiation
in
anionic
polymerizations.
Macromolecules,
Journal Year:
2020,
Volume and Issue:
53(17), P. 7479 - 7486
Published: Aug. 24, 2020
Thermoplastic
elastomers
(TPEs)
based
on
polystyrene
(PS)
are
commonplace
in
society.
The
elastomeric
properties
of
these
materials
often
sacrificed
to
increase
mechanical
such
as
stiffness,
strength,
and
toughness.
We
sought
produce
stiff,
strong,
tough
TPEs
that
retain
their
by
shifting
the
lamellar
phase
boundary
toward
higher
PS
content.
By
precisely
controlling
molecular
weight
distribution
(MWD)
shape
one
block
polystyrene-block-polyisoprene-block-polystyrene
(SIS),
we
produced
continuous
at
atypically
high
volume
fractions,
from
0.33
triblocks
with
a
narrow
MWD
∼0.39
broadened
block.
Furthermore,
observed
hexagonal/lamellar
coexistence
fraction
0.39
when
first
was
asymmetric.
These
exhibit
enhanced
consistent
fractions
morphologies.