Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 27, 2024
We
have
prepared
and
characterized
two
diradicaloid
systems
5a
5b
that
originated
from
the
oxidation
of
a
1,7-(4-(2,6-di-tert-butyl)phenol)-substituted
aza-BODIPY
core.
The
diradicaloids
were
by
large
array
experimental
computational
methods.
diamagnetic
closed-shell
state
was
postulated
as
ground
in
solution
solid-state
with
substantial
thermal
population
originating
both
open-shell
diradical
triplet
states
observed
at
room
temperature.
Transient
absorption
spectroscopy
indicates
fast
(<10
ps)
excited
deactivation
pathways
associated
target
compounds'
character
Variable-temperature
1H
NMR
spectra
indicate
solvent
dependency
5b.
could
be
stepwise
reduced
to
mixed-valence
radical-anion
dianion
upon
consequent
single-electron
reductions.
Similarly,
deprotonated
aza-BODIPYs
can
oxidized
form.
Both
dianionic
forms
exhibit
an
intense
NIR
region.
Density
functional
theory
(DFT)
time-dependent
DFT
calculations
used
explain
transformations
UV–Vis-NIR
all
compounds.
Solar RRL,
Journal Year:
2024,
Volume and Issue:
8(12)
Published: May 17, 2024
Perovskite
solar
cells
(PSCs)
have
become
a
research
hotspot
since
their
dramatic
increase
in
power
conversion
efficiency
(PCE),
surpassing
26%
due
to
advances
cell
engineering
and
interfacial
layers.
Within
the
last
factor,
hole
transporting
materials
play
crucial
role
enhancing
device
performance
stability.
Among
several
molecular
building
blocks,
BODIPYs
are
attractive
for
design
of
novel
material
(HTMs)
outstanding
photophysical
charge
transport
properties
easily
tuned
by
synthetic
modifications.
Herein,
synthesis
five
new
BODIPY‐based
HTMs
PyBDP
1–5
reported,
functionalized
at
meso‐
α‐
positions
with
pyrenyl
arylamino
units,
respectively.
The
resulting
compounds
exhibit
broad
absorption
visible
region,
remarkable
thermal
stability,
narrow
bandgaps,
suitable
energy
levels,
good
extraction
capability,
as
subtracted
from
experimental
computational
characterizations.
BODIPY
derivatives
is
evaluated
planar
inverted
(p‐
i
‐n)
PSCs
compared
commonly
used
PTAA,
highly
efficient
systems,
reaching
PCEs
very
close
that
obtained
reference
polymer
(21.51%).
incorporation
these
result
an
PCE
20.37%
devices
including
PyBDP‐1
19.97%
devises
containing
PyBDP‐3
,
thus
demonstrating
promising
alternative
obtain
simple
organic
HTMs.
Journal of Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
67(17), P. 15908 - 15924
Published: Aug. 21, 2024
In
this
work,
various
novel
pyridinyl-
and
pyridinium-modified
Aza-BODIPY
PSs
were
designed
constructed
based
on
monoiodo
(BDP-4
BDP-15)
in
an
attempt
to
construct
"structure-inherent
organelles-targeted"
endow
potential
organelle-targeting
ability.
Pyridinyl
displayed
potent
photodynamic
efficacy,
monorigidified
very
effective.
The
PS
20
with
meta-pyridinyl
moiety
the
most
photoactivity
negligible
dark
toxicity
a
favorable
dark/phototoxicity
ratio
(>4800).
To
our
surprise,
(e.g.,
20)
was
lipid
droplet-targeted.
showed
good
cellular
uptake
intracellular
ROS
generation
compared
BDP-15.
preliminary
cell
death
process
exploration
indicated
that
resulted
peroxidation
induced
through
iron-independent
ferroptosis-like
pathway.
vivo
antitumor
efficacy
experiments
manifested
significantly
inhibited
tumor
growth
outperformed
BDP-15
Ce6
even
under
single
low-dose
light
irradiation
(30
J/cm2).
Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 27, 2024
We
have
prepared
and
characterized
two
diradicaloid
systems
5a
5b
that
originated
from
the
oxidation
of
a
1,7-(4-(2,6-di-tert-butyl)phenol)-substituted
aza-BODIPY
core.
The
diradicaloids
were
by
large
array
experimental
computational
methods.
diamagnetic
closed-shell
state
was
postulated
as
ground
in
solution
solid-state
with
substantial
thermal
population
originating
both
open-shell
diradical
triplet
states
observed
at
room
temperature.
Transient
absorption
spectroscopy
indicates
fast
(<10
ps)
excited
deactivation
pathways
associated
target
compounds'
character
Variable-temperature
1H
NMR
spectra
indicate
solvent
dependency
5b.
could
be
stepwise
reduced
to
mixed-valence
radical-anion
dianion
upon
consequent
single-electron
reductions.
Similarly,
deprotonated
aza-BODIPYs
can
oxidized
form.
Both
dianionic
forms
exhibit
an
intense
NIR
region.
Density
functional
theory
(DFT)
time-dependent
DFT
calculations
used
explain
transformations
UV–Vis-NIR
all
compounds.