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S1
Electronic Supplementary Information (ESI) For
AIE-active tetraphenylethene functionalized metal-organic framework for
selective detection of nitroaromatic explosives and organic photocatalysis
H2-mtpdc (33 mg, 0.1 mmol) and ZrCl4 (51 mg, 0.22 mmol) were dissolved in DMF (75 mL), which
was added into a 250 mL round bottom flask with a magnetic stir bar. Then, 3.1 mL HAc was added
to the reaction flask and the reaction mixture was heated at 100 °C for 72 hours under an argon
atmosphere. After cooling to room temperature, the product was separated by centrifugal to afford
the white solid which was washed with DMF (100 mL x 3) and EtOH (100 mL x 3), respectively.
The sample was dried in vacuum. The powder X-ray diffraction (PXRD) pattern of product was
similar to the simulated pattern generated from single crystal data (Fig. S1 and S2), confirming its
UiO-68 topological framework and the phase purity. The molar ratio of etpdc to mtpdc in MOF
UiO-68-mtpdc/etpdc was determined to be 1:1.2. In addition, through the varying the feeding ratio of
H2-etpdc and H2-mtpdc, another two MOF samples with different ratio of linkers were prepared by
the similar procedure (UiO-68-mtpdc/etpdc’ and UiO-68-mtpdc/etpdc” refer to 1:2.2 and 1:0.57 the
ratio of H2-etpdc and H2-mtpdc).
Fig. S1 PX
Fig. S2 The z
and UiO-68
Sc
XRD patterns
zoomed-in co
8-mtpdc (bott
tiny shift
cheme S2. Sy
s of MOF as-
omparison of
tom). The pos
may be cause
ynthesis of 1:
synthesized a
contain
f PXRD patte
sition of main
ed by the larg
10 20
2
5
2
1
23
S5
1 mixed strut
and activated
ns H2-mtpdc
erns (2Theta =
n peaks (1-10
ge ligand H2-e
0 30
activ
as-synthes
2Theta / degre
as-s
10
2Theta /degre
4 5
6 7 8
t MOF UiO-6
UiO-68-mtp
linker.)
= 3-20°) of as
0) matches ve
etpdc in MOF
40
vated UiO-68-mtpd
sized UiO-68-mtpd
ee
simulated
synthesized UiO-68
15
ee
89
68-mtpdc/etpd
dc/etpdc. (M
s-synthesized
ry well. The v
F UiO-68-mtp
50
dc/etpdc
dc/etpdc
d UiO-68
8-mtpdc
20
10
dc.
MOF UiO-68-m
d UiO-68-mtp
variation of i
tpdc/etpdc.
mtpdc only
pdc/etpdc (top
intensity and
p)
Fig. S3 1H
H2-mtpdc in
ratio of aro
content
Fig. S4 TGA
of activate
0
40
60
80
100
We
igh
t /
%
H NMR of dig
as-prepared
ound 1:1.2, w
of H2-mtpdc
A plot of as-sy
ed sample can
200
Te
gested UiO-68
MOF was ca
which is almo
linker in MO
ynthesized (l
n be attributed
f
400
emperature / o
8-mtpdc/etpd
alculated from
st same to the
OF should be
eft) and deso
d to the re-ad
framework ca
600oC
S6
dc by HF in D
m the integrati
e initial ratio
ascribed to th
olvated (right)
dsorbed water
an be stable u
800
Wei
gh
t /
%
DMSO-d6. Th
ion of He (H2
of 1:1 in prep
he steric bulk
) MOF UiO-6
r during samp
up to ~500 °C
040
60
80
100
e molar ratio
2-etpdc) and H
paration of M
k of TPE moie
68-mtpdc/etpd
ple weighing
C.
200 4
Tempera
o of linkers H2
H2 (H2-mtpd
MOF. The slig
ety of H2-etpd
dc. The initia
in air. This su
00 600
ature / oC
2-etpdc and
dc), giving the
ghtly higher
dc linker.
al weight loss
uggests the
800
e
s
Fig.
Fig
Fig. S7 Em
00
100
200
300
Nit
rog
en a
t S
TP
/ cm
3 g-1
S5 Nitrogen
g. S6 Photogr
mission spect
.0 0.2
Re
adsorptio desorptio
sorption isoth
raphs of MOF
tra of ligand H
0.4 0.6
elative Pressur
onon
4
No
rmal
ized
In
ten
sit
y
herm at 77 K
UiO
F UiO-68-mtp
H2-etpdc and
0.8 1.
re P/P0
400 50
W
S7
K (left) and BE
O-68-mtpdc/et
pdc/etpdc und
MOF UiO-6
.0
1/[W
((P
0/P
)-1)
]
00 60
Wavelength /
ET specific su
tpdc.
der daylight (
68-mtpdc/etpd
0.020.08
0.12
0.16
0.20
00 70
nm
ligand H2-etpdc MOF UiO-68-mtpd
urface area pl
(left) and 365
dc in solid sta
0.03
Relative P
00
dc/etpdc
lot (right) of
5 nm light (rig
ate at room te
0.04
SBET = 960 m2
Pressure P/P0
MOF
ght).
emperature.
0.05
2 g-1
Table S1. Ph
H2-etp
UiO-6
UiO-6
UiO-6
Fig. S8 Ph
hotophysical p
pdc
68-mtpdc/etpdc
68-mtpdc/etpdc
68-mtpdc/etpdc
hotographs of
parameters fo
λem, max, n
518
c 490
c’ 488
c” 491
f ligand H2-etp
or ligand H2-e
for
nm Φ, %
32
48
41
53
S8
tpdc under da
etpdc and MO
r TNP and DN
lifetime, n
τ1 1.83
τ1 1.96
aylight (left) a
OFs as well a
NP.
ns (% contribut
(48), τ2 5.15 (5
(55), τ2 5.11 (4
-
-
and 365 nm li
as their quenc
tion)
2)
5) 2.8
2.9
2.6
ight (right).
ching effect c
ksv, 104 M-1
-
(TNP), 2.3 (DN
(TNP), 2.5 (DN
(TNP), 2.0 (DN
coefficient (ks
NP)
NP)
NP)
sv)
Fig. S9 1H N
and H2-
Fig. S10 1H
and H2-
NMR of dige
-mtpdc in as-
NMR of dige
mtpdc in as-p
ested UiO-68-
-prepared MO
ested UiO-68
prepared MO
-mtpdc/etpdc
OF to be 1:2.2
-mtpdc/etpdc
OF to be 1:0.5
S9
c’ by HF in D
2 from the int
c” by HF in D
7 from the in
MSO-d6, giv
tegration of H
DMSO-d6, giv
ntegration of H
ing the molar
He (H2-etpdc)
ving the mola
He (H2-etpdc
r ratio of link
) and H2 (H2-
ar ratio of link
c) and H2 (H2
kers H2-etpdc
-mtpdc).
kers H2-etpdc
2-mtpdc).
c
S10
Fig. S11 Emission spectra of MOF UiO-68-mtpdc/etpdc dispersed in CH3OH (0.02 mg/mL) upon incremental
addition of DNP (left); and the corresponding Stern-Volmer plot of the quenching fluorescence intensity as a
function of DNP concentration (right, ksv = 2.3 × 104 M-1).
Fig. S12 Emission spectra of MOF UiO-68-mtpdc/etpdc dispersed in CH3OH (0.02 mg/mL) upon incremental
addition of p-NP (left); and the corresponding Stern-Volmer plot of the quenching fluorescence intensity as a
function of p-NP concentration (right, ksv = 7.2 × 103 M-1).
400 450 500 550 600 6500
200
400
600
800
1000
Inte
ns
ity
/ a
.u.
Wavelength / nm
0
100 M
DNP
10 20 30 40 50
0.3
0.6
0.9
1.2
1.5
(I0/
I) -
1
Concentration / M
400 450 500 550 600 6500
200
400
600
800
1000
Inte
nsi
ty /
a.u
.
Wavelength / nm
0
100 M
p-NP
10 20 30 40 500.0
0.1
0.2
0.3
0.4
(I0/
I) -
1
Concentration / M
Fig. S13 Fl
UiO-68-mtpd
2,4,6-trinitro
2,4-dinitrotol
(p-NT), nitro
luorescence q
dc/etpdc (0.0
phenol (TN
luene (DNT)
obenzene (NB
quenching in
02 mg/mL)
NP), 2,4-din
, 1,3-dinitrob
B).
nduced after
in CH3OH
itrophenol (
benzene (DNB
S11
r addition of
under a U
(DNP), p-n
B), o-nitrotolu
f various nit
UV lamp (36
nitrophenol (
uene (o-NT),
troaromatic c
65 nm). Fro
(p-NP), 2,4
m-nitrotolue
compounds
om left to
4,6-trinitrotolu
ene (m-NT), p
(0.1 mM) to
right: blank
uene (TNT)
p-nitrotoluene
o
k,
),
e
Computa
For simplif
software.[S3
functional w
center, Dep
Frequencie
correspond
Fig. S14 T
energy-minim
d(H79-N39) =
ational De
fying the co
3] Density
with the 3-2
partment o
s were also
ed to a min
The optimized
mized structu
= 1.01 Å, d(O
etails
omputation,
functional
21G basis s
of Chemistr
o calculated
imum on th
d complex str
ure are listed b
O16-N38) = 2.5
we only us
theory (DF
set. Four pr
ry, Beijing
d at the sam
he potential
ructure betwe
below (d: dis
59 Å, θ(O16-H
blue, gray
S12
se TNP and
FT) calcula
rocessing co
Normal U
me level of
energy surf
een TNP and
stance; θ: bon
H19-N38) = 15
and white, re
d etpdc-link
tions were
ores and 8 G
University)
f theory to
face.
etpdc-linker.
nd angle): d(O
6o. Oxygen, n
espectively.
ker for calcu
performed
GB physica
were used
ensure that
Several impo
O16-H19) = 1.5
nitrogen, carb
ulation by G
d by using
al memory
for the o
t each stati
ortant parame
58 Å, d(H19-N
bon and hydro
Gaussian 09
the B3LYP
(Computing
ptimization
ionary poin
eters of the
N38) = 1.07 Å
ogen are red,
9
P
g
n.
nt
Å,
S13
General procedure for Aerobic CDC reactions of tetrahydroisoquinolines 1 with indoles 2
catalyzed by UiO-68-mtpdc/etpdc: The weighed photocatalyst UiO-68-mtpdc/etpdc (2 mg), 1 (0.1
mmol) and 2 (0.3mmol) were added into 2 mL CH3OH. The reaction mixture with stirring was
irradiated by blue LEDs for 12 hours under air at room temperature. 1H NMR spectroscopy was
employed to determine the yield; and 1H NMR spectra of products 3 are in agreement with reported
literature.[S4] The catalyst for cyclic reaction was recycled by centrifugation at 10 000 rpm and
washed by fresh CH3OH two times.
Table S2 Screening of the model CDC reaction conditionsa
Entry Conditions Solvent Time (h) Yield (%)b
1 UiO-68-mtpdc/etpdc, 1 mg CH3OH 8 41
2 UiO-68-mtpdc/etpdc, 1 mg CH3OH 12 68
3 UiO-68-mtpdc/etpdc, 2 mg CH3OH 8 72
4
5
6
UiO-68-mtpdc/etpdc, 2 mg
UiO-68-mtpdc/etpdc’, 2mg
UiO-68-mtpdc/etpdc”, 2mg
CH3OH
CH3OH
CH3OH
12
12
7
93
79
92
7 UiO-68-mtpdc/etpdc, 2 mg CH3CN 12 87
8 UiO-68-mtpdc/etpdc, 2 mg DMF 12 83
9 No catalyst CH3OH 12 trace
10 In dark CH3OH 12 trace
11
12
In N2 atmosphere
In O2 atmosphere
CH3OH
CH3OH
12
7
trace
90
13c UiO-68-mtpdc, 2 mg CH3OH 12 trace
14d UiO-68-mtpdc/etpdc, 2 mg CH3OH - 61
aReaction conditions: 1a (0.1 mmol) and 2a (0.3 mmol), blue LEDs (λmax = 450 nm), solvent (2
mL). The reaction with stirring was conducted in air at room temperature. bDetermined by 1H NMR. cMOF UiO-68-mtpdc only contains ligand H2-mtpdc.[S1] dAfter 5 h reaction the MOF was filtered
out (yield: 58%) and the filtrate went on for another 8 hours.
S14
Table S3 The aerobic CDC reactions of tetrahydroisoquinolines 1 with indoles 2 photocatalyzed by
UiO-68-mtpdc/etpdc a
aReaction conditions: 1 (0.1 mmol), 2 (0.3 mmol) and UiO-68-mtpdc/etpdc (2 mg) in CH3OH (2
mL) under air at room temperature with 12 h blue LEDs (λmax = 450 nm) irradiation. Yields were
determined by 1H NMR.
S15
Table S4 The aerobic CDC reactions of tetrahydroisoquinolines 1 with nitroalkanes 4 photocatalyzed by
UiO-68-mtpdc/etpdc a
aReaction conditions: 1 (0.1 mmol) and 4 (1 mL), blue LEDs (λmax = 450 nm). The reaction with
stirring was conducted in air at room temperature. Yields were determined by 1H NMR.
Fig. S15 Recycling experiments of UiO-68-mtpdc/etpdc for the reaction of N-phenyltetrahydroisoquinoline and
indole.
NAr
NAr
1 4 5
UiO-68-mtpdc/etpdc
blue LEDs, airR4 NO2
NO2R4
1 2 3 4 50
20
40
60
80
100
Yie
ld /
%
Run times
S16
Fig. S16 PXRD patterns of MOF UiO-68-mtpdc/etpdc after photocatalysis.
Fig. S17 EPR measurements of a solution in CH3OH of UiO-68-mtpdc/etpdc without 1a (a) and with 1a (b) in the
presence of TEMP upon the irradiation of blue LEDs for 30 s; a solution in CH3OH of UiO-68-mtpdc/etpdc without
1a (c) and with 1a (d) in the presence of DMPO upon the irradiation of blue LEDs for 30 s. In O2 atmosphere.
Scheme S3 Proposed mechanism for the photocatalytic aerobic CDC reaction of N-phenyltetrahydroisoquinoline
and indole by MOF UiO-68-mtpdc/etpdc (photocatalyst, PC). ESI-MS was used to capture the intermediate of
imine cation and peroxide species. Also, the main product and by-product were observed in ESI-MS spectra.