Green Chemistry,
Год журнала:
2023,
Номер
25(23), С. 9998 - 10009
Опубликована: Янв. 1, 2023
This
work
provides
a
strategy
for
synthesizing
PGA-PBC-PGA
triblock
copolymers
and
allows
the
recovery
of
GL
within
3.0
h
through
depolymerization
in
an
82%
yield.
Macromolecules,
Год журнала:
2023,
Номер
56(15), С. 6019 - 6026
Опубликована: Июль 22, 2023
The
development
of
chemically
recyclable
polymers
with
closed-loop
life
cycles
is
believed
to
be
the
most
attractive
strategy
in
creating
circular
plastic
economy.
Here,
we
successfully
prepared
a
pair
enantiopure
O-heterocyclic
lactones
bearing
pendent
phenyl
substituent,
which
are
named
(2S,7R)-7-methyl-2-phenyl-1,4-dioxepan-5-one
(SR-M1)
and
(2R,7R)-7-methyl-2-phenyl-1,4-dioxepan-5-one
(RR-M2),
respectively,
by
using
methanolysis
product
poly(3-hydroxybutyrate)
(P3HB)
as
raw
material.
well-controlled
ring-opening
polymerizations
SR-M1
RR-M2
were
achieved
presence
MeAl[salen]
catalyst
produce
poly(ether-ester)s
controlled
molecular
weights,
narrow
dispersities,
well-defined
terminal
groups.
monomer
stereoconfiguration
has
big
impact
on
their
polymerization
kinetics
thermodynamics
well
thermal
mechanical
properties
resultant
polyesters.
Both
P(SR-M1)
P(RR-M2)
exhibited
recyclability.
depolymerization
polyesters
back
pristine
monomers
can
easily
realized
stannous
octoate
solution.
Fundamental Research,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 1, 2024
The
development
of
modern
society
is
closely
related
to
polymer
materials.
However,
the
improper
disposal
wastes
not
only
squanders
resources
but
also
intensifies
environmental
issues,
despite
that
energy
recovery,
physical
recycling
and
chemical
pathways
have
been
developed
tackle
recycle
reuse
polymers.
Among
them,
considered
as
most
pivotal
solution,
it
can
depolymerize
back
monomers,
which
then
repolymerize
into
Recently,
remarkable
progress
has
made
in
chemically
recyclable
polymers
through
monomer
design
shift
"polymerization-depolymerization"
equilibrium
realize
selective
depolymerization
achieve
closed-loop.
This
article
reviews
closed-loop
such
polyesters,
polycarbonates,
sulfur-containing
polymers,
vinyl
monomer-based
well
other
types
Moreover,
challenges
prospects
this
field
are
discussed.
Chemical Communications,
Год журнала:
2024,
Номер
unknown
Опубликована: Янв. 1, 2024
Progress
in
chemical
recycling
of
waste
polyesters
(waste
plastic
refinery)
was
reviewed
and
prospected,
newly
reported
thermal
catalysis,
photocatalysis,
electrocatalysis,
biocatalysis
the
recycle
PET-based
product
were
introduced.
Chinese Journal of Chemistry,
Год журнала:
2022,
Номер
40(24), С. 2973 - 2980
Опубликована: Сен. 5, 2022
Comprehensive
Summary
Monomer
design
strategy
has
become
a
powerful
tool
to
access
polymers
with
desired
and
diverse
functionalities.
Here,
we
designed
novel
monomer
2‐((benzyloxy)methyl)‐1,4‐oxathiepan‐7‐one
(BTO)
via
installing
benzyl
ether
side
chain
the
structure
of
1,4‐oxathiepan‐7‐one
(OTO).
The
ring‐opening
polymerization
BTO
Zn1
as
catalyst
demonstrated
characteristics
living
turnover
frequency
(TOF)
up
2520
h
−1
.
With
[BTO]
0
/[
]
/[I]
feed
ratio
2000/2/1,
polymer
high
number‐average
molecular
weight
(
M
n
=
536
kDa)
narrow
dispersity
Ð
1.06)
was
obtained.
produced
glass
transition
temperature
‐17°C
behaved
an
elastomer
at
room
temperature.
Consequently,
copolymerized
L
‐LA
modulate
mechanical
properties
P(
‐LA).
When
content
is
10%,
copolymer
exhibits
excellent
strength
(24
MPa)
elongation
break
(270%),
affording
crystalline,
hard,
tough
plastic
material
that
combines
ductility
P(BTO)
modulus
In
addition,
oxidation
P(BTO)‐SO
2
led
improvement
T
g
from
38°C.
Debenzylation
afforded
‐OH
containing
free
hydroxyl
groups.
Ultimately,
could
be
hydrolyzed
under
base
condition
recover
corresponding
acid
intermediate,
which
used
prepare
again
complete
closed‐loop
monomer.
Chemistry - An Asian Journal,
Год журнала:
2022,
Номер
18(3)
Опубликована: Дек. 15, 2022
The
low
temperature
condition,
long
reaction
time
and
associated
high
energy
inputs
involved
in
the
polymerization
process
still
hampered
scalable
production
of
poly(γ-butyrolactone)
(PγBL)
via
ring-opening
(ROP)
strained
γBL
due
to
its
unfavorable
thermodynamics.
In
this
contribution,
we
presented
rapid
ROP
using
a
bisurea
combination
with
an
organophosphazene
base
as
binary
catalyst.
Well-defined
PγBL
samples
various
terminal
groups
were
prepared
by
different
alcohol
initiators.
co-catalyst
exhibited
much
higher
catalytic
activity
even
compared
most
active
monourea
previous
report
supported
kinetic
experiments.
A
moderate
monomer
conversion
61%
was
achieved
within
10
mins,
producing
high-molecular-weight
Mn
up
37.5
kDa
good
mechanical
properties.
short
considerably
reduced
cost
for
conducted
at
condition.
This
study
may
clear
away
obstacles
practical
applications
PγBL.
Chemistry - An Asian Journal,
Год журнала:
2023,
Номер
18(7)
Опубликована: Фев. 9, 2023
A
fully
renewable
bio-based
bicyclic
lactone
containing
a
five-membered
cyclic
ketal
moiety,
7-methyl-3,8,10-trioxabicyclo[5.2.1]decan-4-one
(TOD),
was
synthesized
through
two-step
acid-catalyzed
process
from
glycerol
and
levulinic
acid.
The
ring-opening
polymerization
(ROP)
of
TOD
at
30°C
with
benzyl
alcohol
(BnOH)
as
the
initiator
1,5,7-triazabicyclo[4.4.0]dec-5-ene
(TBD)
catalyst
can
afford
high
molar
mass
PTOD
cis-2.4-disubstitued
2-methyl
1,3-dioxolane
moiety
in
its
repeating
unit.
is
an
amorphous
polymer
glass
transition
temperature
(Tg
)
13°C.
It
be
hydrolyzed
into
structurally
defined
small
molecules
under
acidic
or
basic
conditions
by
selective
cleavage
either
ester
linkage
respectively.
TBD-catalyzed
copolymerization
L-lactide
(L-LA)
-20°C
investigated.
confirmed
that
L-LA
polymerized
quickly
racemization
to
form
PLA,
followed
slow
incorporation
formed
PLA
chains
via
transesterification.
By
varying
feed
ratios
TOD,
series
random
copolymers
(PLA-co-PTOD)
different
tunable
Tg
s
were
obtained.
Under
conditions,
PLA-co-PTOD
degrades
much
faster
than
linkages.
This
work
provides
insights
for
development
more
sustainable
acid-accelerated
degradable
alternatives
aliphatic
polyesters.
Current Opinion in Green and Sustainable Chemistry,
Год журнала:
2022,
Номер
37, С. 100656 - 100656
Опубликована: Июль 7, 2022
Polyhydroxyalkanoates
(PHAs)
are
currently
discussed
as
renewably
sourced
alternatives
for
fossil-based
plastics.
With
microbial
PHA
production
evolving
into
a
more
mature
technology,
new
opportunities
arise
to
use
these
materials
beyond
the
application
biopolymers.
For
example,
C4
chiral
hydroxy
acid
backbone
of
most
abundant
and
readily
available
PHA,
poly(3-hydroxybutyrate)
(PHB),
renders
it
an
attractive
circular
carbon
feedstock
synthesis
many
polymers
or
value-added
platform
molecules
such
crotonic
(R)-3-hydroxybutyric
acid.
The
respective
C4-platform
is
particularly
promising
current
(bio)refinery
options
functionalized
C4-monoacids
limited
show
narrower
product
scope
than
sugar-based
C3-
C5-platforms.
This
concept
expected
translate
well
other
PHAs
containing
microbially
customizable
chain
length
(C3-C14),
further
broadening
portfolio
building
blocks.