Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(34)
Published: June 12, 2024
Abstract
Stimuli‐responsive
physisorbents
that
undergo
reversible
structural
transformations
induced
by
external
stimuli
(e.g.
light,
guests,
or
heat)
offer
the
promise
of
utility
in
gas
storage
and
separation.
Whereas
reports
on
guest
light‐responsive
sorbents
have
increased
recent
years,
we
are
unaware
exhibit
both
light
guest‐induced
transformations.
Herein,
report
square
lattice,
sql
,
topology
coordination
network
Zn(fba)(bis)
⋅
2DMF
(
sql‐5,6‐Zn‐α
5=trans‐4,4′‐bis(1‐imidazolyl)stilbene=bis,
6=2,2‐bis(4‐carboxyphenyl)hexafluoropropane=H
2
fba)
underwent
single‐crystal‐to‐single‐crystal
transformation
(SCSC)
upon
activation,
affording
nonporous
sql‐5,6‐Zn‐β
.
Parallel
alignment
at
3.23
Å
olefinic
moieties
adjacent
bis
ligands
enabled
SCSC
[2+2]
photocycloaddition
exposure
to
UV
(365
nm)
sunlight.
thereby
transformed
mot‐5,6‐Zn‐α
which
was
subsequently
activated
narrow
pore
phase
mot‐5,6‐Zn‐β
exhibited
S‐shaped
adsorption
isotherms
characteristic
changes
when
exposed
CO
195
K
(type‐F–IV
type
F–I,
respectively).
Cycling
experiments
conducted
reduced
particle
size
after
cycle
1
into
a
rare
example
shape
memory
network,
sql‐5,6‐Zn‐γ
Insight
this
smorgasbord
gained
from
situ
PXRD,
single
crystal
XRD
H
NMR
spectroscopy
experiments.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(25)
Published: April 17, 2024
Zeolitic
octahedral
metal
oxide
is
a
newly
synthesized
all-inorganic
zeolitic
material
and
has
been
used
for
adsorption,
separation,
catalysis.
Herein,
new
was
characterized.
The
porous
framework
established
through
the
assembly
of
[P
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(25)
Published: April 17, 2024
Abstract
Zeolitic
octahedral
metal
oxide
is
a
newly
synthesized
all‐inorganic
zeolitic
material
and
has
been
used
for
adsorption,
separation,
catalysis.
Herein,
new
was
characterized.
The
porous
framework
established
through
the
assembly
of
[P
2
Mo
13
O
50
]
clusters
with
PO
4
linkers.
Guest
molecules
occupied
framework,
which
could
be
removed
heat
treatment,
thereby
opening
micropores.
pore
characteristics
were
controlled
by
cations
within
micropore,
enabling
adjustment
interactions
alkynes
alkenes.
This
resulted
in
good
separation
performance
ethylene/acetylene
propylene/propyne
even
under
high
temperature
humidity
conditions.
stability
enabled
efficient
recovery
reuse
without
discernible
loss
performance.
Due
to
relatively
weak
interaction
between
adsorbed
alkyne
adsorbent
facilitated
highly
pure
alkyne.
feature
enhances
practical
applicability
various
industrial
processes.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(34)
Published: June 12, 2024
Abstract
Stimuli‐responsive
physisorbents
that
undergo
reversible
structural
transformations
induced
by
external
stimuli
(e.g.
light,
guests,
or
heat)
offer
the
promise
of
utility
in
gas
storage
and
separation.
Whereas
reports
on
guest
light‐responsive
sorbents
have
increased
recent
years,
we
are
unaware
exhibit
both
light
guest‐induced
transformations.
Herein,
report
square
lattice,
sql
,
topology
coordination
network
Zn(fba)(bis)
⋅
2DMF
(
sql‐5,6‐Zn‐α
5=trans‐4,4′‐bis(1‐imidazolyl)stilbene=bis,
6=2,2‐bis(4‐carboxyphenyl)hexafluoropropane=H
2
fba)
underwent
single‐crystal‐to‐single‐crystal
transformation
(SCSC)
upon
activation,
affording
nonporous
sql‐5,6‐Zn‐β
.
Parallel
alignment
at
3.23
Å
olefinic
moieties
adjacent
bis
ligands
enabled
SCSC
[2+2]
photocycloaddition
exposure
to
UV
(365
nm)
sunlight.
thereby
transformed
mot‐5,6‐Zn‐α
which
was
subsequently
activated
narrow
pore
phase
mot‐5,6‐Zn‐β
exhibited
S‐shaped
adsorption
isotherms
characteristic
changes
when
exposed
CO
195
K
(type‐F–IV
type
F–I,
respectively).
Cycling
experiments
conducted
reduced
particle
size
after
cycle
1
into
a
rare
example
shape
memory
network,
sql‐5,6‐Zn‐γ
Insight
this
smorgasbord
gained
from
situ
PXRD,
single
crystal
XRD
H
NMR
spectroscopy
experiments.
Chemistry of Materials,
Journal Year:
2024,
Volume and Issue:
36(21), P. 10710 - 10719
Published: Oct. 18, 2024
Tailoring
a
MOF
with
suitable
pore
windows
for
the
sieving
C3H6/C3H8
separation
is
attractive
but
challenging,
where
controlling
local
framework
flexibility
by
introducing
functionality
provides
solution.
In
this
work,
four
isoreticular
ultramicroporous
Zn–triazolate–dicarboxylate
frameworks,
Zn-ATZ-IP(R)
(R
=
−F,
−OH,
−NH2,
and
−CH3)
(HATZ
3-amino-1,2,4-triazole;
H2IP-R
R
group
functionalized
isophthalic
acid)
variable
apertures,
were
targeted
as
platforms
to
study
effect
of
functional
groups
on
their
performance.
Single-component
adsorption
isotherms
uncovered
potential
Zn-ATZ-IP(OH)-a
hydroxyl
adsorbent.
Single
X-ray
diffraction
(SXRD)
measurements
revealed
that
strong
intraframework
hydrogen
bonds
hinder
free
torsion
ATZ–
ligand
in
Zn-ATZ-IP(OH)-a,
defining
rigid
admit
C3H6
while
exclude
C3H8,
whereas
other
give
adaptive
larger
pores
allow
both
C3H8
in.
Further,
situ
XRD
suggested
temperature
alters
strength
bonds,
making
ideal
room-temperature
C3H6/C3H8.
This
work
highlights
superiority
customizing
sustained
which
advances
rational
design
smart
adsorbents
energy-efficient
light
hydrocarbon
separations.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(34)
Published: June 12, 2024
Abstract
Stimuli‐responsive
physisorbents
that
undergo
reversible
structural
transformations
induced
by
external
stimuli
(e.g.
light,
guests,
or
heat)
offer
the
promise
of
utility
in
gas
storage
and
separation.
Whereas
reports
on
guest
light‐responsive
sorbents
have
increased
recent
years,
we
are
unaware
exhibit
both
light
guest‐induced
transformations.
Herein,
report
square
lattice,
sql
,
topology
coordination
network
Zn(fba)(bis)
⋅
2DMF
(
sql‐5,6‐Zn‐α
5=trans‐4,4′‐bis(1‐imidazolyl)stilbene=bis,
6=2,2‐bis(4‐carboxyphenyl)hexafluoropropane=H
2
fba)
underwent
single‐crystal‐to‐single‐crystal
transformation
(SCSC)
upon
activation,
affording
nonporous
sql‐5,6‐Zn‐β
.
Parallel
alignment
at
3.23
Å
olefinic
moieties
adjacent
bis
ligands
enabled
SCSC
[2+2]
photocycloaddition
exposure
to
UV
(365
nm)
sunlight.
thereby
transformed
mot‐5,6‐Zn‐α
which
was
subsequently
activated
narrow
pore
phase
mot‐5,6‐Zn‐β
exhibited
S‐shaped
adsorption
isotherms
characteristic
changes
when
exposed
CO
195
K
(type‐F–IV
type
F–I,
respectively).
Cycling
experiments
conducted
reduced
particle
size
after
cycle
1
into
a
rare
example
shape
memory
network,
sql‐5,6‐Zn‐γ
Insight
this
smorgasbord
gained
from
situ
PXRD,
single
crystal
XRD
H
NMR
spectroscopy
experiments.