recognition of Cu2+ and F : Effect of functional group on ... · Selective Chromo …. Soumen et...
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Supporting Information
Selective Chromo-fluorogenic molecular sensor for dual channel
recognition of Cu2+ and F–: Effect of functional group on selectivity
Soumen Ghosha, Aniruddha Gangulya, Arghadeep Bhattacharyyaa, Md. Akhtarul Alamb*,
and Nikhil Guchhaita*
aDepartment of Chemistry
University of Calcutta
92, A.P.C. Road, Kolkata 700 009, India
Telephone 91-33-23508386
Fax: 91-33-23519755
bDepartment of Chemistry
Aliah University
IIA/27, New Town, Kolkata-700 156, West Bengal, India
*Corresponding author, E-mail: [email protected] (M. A. A.)
and
[email protected] (N.G.)
Electronic Supplementary Material (ESI) for RSC Advances.This journal is © The Royal Society of Chemistry 2016
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Table of Contents
1. Syntheses and characterization...….…......................…..... S3
2. Naked-eye color change…………………………………….S12
3. UV–vis Spectra………………………….……………..........S13
4. Fluorescence Spectra…………………………. …….…..... S19
5. Optimized structure………………………………………….S22
6. Interference of ions…………………………………………..S23
7. Toothpaste test…….………………………………………….S28
8. Mechanism…………………………….…………….….........S30
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1. Synthesis
1.1. Syntheses and characterization
Scheme S1. Syntheses of Compounds 1 (HNHCB), 2 (NHCB), and 3(HNHB)
1.2. Compound 2. Sythesis of naphthalene-2-carboxylic acid (4-cyano-benzylidene)-hydrazide (NHCB):
Compound 2 has been prepared according to the similar procedure as compound 1 by
the reaction between naphthalene-2-carboxylic acid hydrazide (1.3 mmol, 0.250 g) and
4-formyl benzonitrile (1.4 mmol, 0.180 g) in methanol. The colourless solid thus
obtained was filtered and then dried under vacuum (yield: 0.32 g, 80%). 1H NMR in d6-
DMSO, 300MHz, δ (ppm): 12.32 (s, 1H, –CONH–), 8.70 (s, 2H, –CH=N– and naph),
8.10-7.96 (m, 8H), 7.68-7.66 (m, 2H), 13C NMR (75.5 MHz, d6-DMSO, 20 ºC) δ (ppm):
111.00, 120.74, 124.22, 126.26, 127.21, 128.74, 129.08, 129.29, 130.07, 134.58, 136.27,
148.95, 154.51, 164.23, 176. IR (KBr): 3390, 3203, 3055, 2860, 2227, 1655, 1637, 1623,
1571, 1503, 1370, 1300, 1238, 1203, 1071 cm–1.
O
NH
N
OHC
+MeOHReflux
R1
R1
X R1Compounds1 –OH –CN
2 –CN–H
3 –H–OH
OHN
NH2
X
X
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1.3. Compound 3. Sythesis of benzylidene 3-hydroxy-naphthalene-2-
carbohydrazide(HNHCB):
Compound 3 has been also prepared according to the similar procedure as compound 1
by the condensation between 3-hydroxy-naphthalene-2-carboxylic acid hydrazide and
benzaldehyde ( yield: 72%). 1H NMR in d6-DMSO, 300MHz, δ (ppm): 12.02 (s, 1H, –
CONH–), ~11.5 (broad, 1H, –OH), 8.48 (s, 2H, –CH=N– and naph), 7.94 (d, J=7.8Hz,
1H), 7.80-7.35 (m, 9H). 13C NMR (75.5 MHz, d6-DMSO, 20 ºC) δ (ppm): 111.04,
116.88, 117.63, 119.06, 119.90, 126.28, 129.08, 129.79, 129.91, 130.74, 132.03, 136.81,
154.50, 157.95, 164.20. IR (KBr): 3242, 3023, 2894, 1659, 1622, 1537, 1487, 1397,
1228, 1213, 1075, 1102, 1070 cm–1.
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2. Characterization
Figure S1. 1H NMR (300 MHz) spectrum of HNHCB in d6-DMSO at 20 ºC
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Figure S2. 13C NMR (300 MHz) spectrum of HNHCB in d6-DMSO at 20 ºC
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Fig. S3. Mass spectra (TOF-MS ES+) of HNHCB
[1+Na]+
[1+H]+
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Figure S4. 1H NMR (300 MHz) spectrum of NHCB in d6-DMSO at 20 ºC
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Figure S5. 13C NMR (300 MHz) spectrum of NHCB in d6-DMSO at 20 ºC
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Figure S6. 1H NMR (300 MHz) spectrum of HNHB in d6-DMSO at 20 ºC
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Figure S7. 13C NMR (300 MHz) spectrum of HNHB in d6-DMSO at 20 ºC
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3. Naked-eye color change
Figure S8. Naked-eye color changes of compound 2 (NHCB) (1.0 10–5 M) after
addition of 2 equivalent of F- and OAc- in acetonitrile water mixture (7:3, v/v).
2
F-
2 + F-
OAc-
2 + OAc-
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4. UV–Vis Spectra
Figure S9. UV–vis spectral changes of HNHCB (1.0 10–6 M) upon addition of OAc–
ion (0–5 equiv.) in acetonitrile water mixture (7:3, v/v).
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Figure S10. UV–vis spectral changes of NHCB (0.5 M) in presence of F– ion (0-
2.5eqv.) in aqueous acetonitrile solvent (7:3, v/v).
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Figure S11. UV–vis spectral changes of NHCB (0.5 M) in presence of AcO– ion (0-
2.5eqv.) in acetonitrile water mixture (7:3, v/v).
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Figure S12. UV–vis spectral changes of HNHB (0.5 M) in presence of F– ion (0-
2.5eqv.) in acetonitrile water mixture (7:3, v/v).
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Figure S13. UV–vis spectral changes of HNHCB (0.5 M) in presence of F–, AcO–,
H2PO4–, Cl–, Br–, HSO3
–, NO3– and CN– ion (0-2.5eqv.) in acetonitrile water mixture (7:3,
v/v).
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HNHCB + Cu2+
HNHCB
HNHCB + other cations
Figure S14. UV–vis spectral changes of HNHCB (0.5 M) in presence of other cations
(Cu2+, Mn2+, Fe2+, Fe3+, Cr3+, Co2+, Ni2+, Zn2+, Cd2+ , Hg2+ , Ca2+, Mg2+, Pb2+ion (0-
2.5eqv.) .) in acetonitrile water mixture (7:3, v/v).
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Figure S15. Emission intensity of HNHCB (0.5 M) (a) in presence of Cu2+, Mn2+, Fe2+,
Fe3+, Co2+, Ni2+, Zn2+, Cd2+ and Hg2+ ion (b) in presence of Pb2+, Ca2+, Mg2+, Cr3+ (0-
2.5eqv.) in acetonitrile water mixture (7:3, v/v).
a
Pb2+, Ca2+, Mg2+
Cr3+HNHCB
HNHCB + other cations
HNHCB + Zn2+
HNHCB + Cu2+
a b
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Figure S16. Benesi–Hildebrand plot for 1:1 complexation of HNHCB -Cu2+ complex
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Figure S17. The fluorescence intensities of HNHCB and HNHCB–Cu2+ at various pH
values at room temperature in acetonitrile water mixture (Tris-HCl buffer, pH = 7.2,
CH3CN–H2O = 7 : 3, v/v)
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Figure S18. Emission intensity of HNHB (0.5 M) in presence of Cu2+ (0-5eqv.) in
acetonitrile water mixture (7:3, v/v).
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1
HNHCB +Cu2+
Figure S19. B3LYP optimized structure of HNHCB (top) and HNHCB –Cu2+ complex
(bottom)
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Cu2+ Mn2+ Zn2+Co2+ Ni2+ Fe2+ Fe3+Hg2+ Cd2+ Pb2+ Ca2+Mg2+Cr3+
HNHCB + Mn+
HNHCB + Mn+ + Cu2+
0
0.1
0.2
0.3
Fl.In
tens
ity(a
.u.)
Figure S20. The selectivity of HNHCB for Cu2+ in the presence of other metal ions in
acetonitrile water mixture (CH3CN–H2O = 7 : 3, v/v), λem = 440 nm
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Figure S21. Fluorescence spectra of HNHCB (1×10−7 M), HNHCB with copper ion
and HNHCB with mixture of ions (Cu2+, Ni2+, Co2+, Mn2+, Fe2+, Cd2+, Hg2 +, Ca2+, Mg2+,
Pb2+, Fe3+, Cr3+, F−, OAc−, H2PO4−, Cl− ,Br−, NO3
− , NO2−, CN-, HSO3
− and HSO4− ) in
acetonitrile water mixture (7:3, v/v)
HNHCB+
Cu2+
HNHCB + Cu2+ + Ni2+ + Co2+ + Mn2+ + Fe2+ + Cd2+ +Hg2 + + Fe3+ + Cr3+ + Ca2+ +
Mg2+ + Pb2+ + F- + Oac- + H2PO4
- + Cl- + Br- + HSO3-
+ NO2- + NO3
- + CN- +HSO4
-
HNHCB
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F− OAc− H2PO4− Cl− Br− NO3
− NO2− HSO3
− CN − HSO4−
HNHCB + X −
HNHCB + X − + F −
0
0.1
0.2
0.3
O.D
. at 3
90
Figure S22. The selectivity of HNHCB for F- in the presence of other anions in
acetonitrile water mixture (CH3CN–H2O = 7 : 3, v/v)
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Figure S23. UV–vis spectral changes of 1(HNHCB) in bare F-and in presence of F- and
Cu2+ mixture in aqueous acetonitrile (7:3, v/v).
1
1+ F-
1 + F- + Cu2+
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Figure S24. UV–vis spectral changes of 1(HNHCB) in bare OAc -and in presence of
OAc- and Cu2+ mixture in aqueous acetonitrile (7:3, v/v).
1
1 + OAc-
1 + OAc- + Cu2+
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Figure S25. Determination of detection limit of Cu2+ by HNHCB (1 10–7) in CH3CN-water mixture at em = 443nm.
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Figure S26. Determination of detection limit of F– by HNHCB (1x 10–6) in water acetonitrile mixture at abs =390nm.
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Fig. S27 Uv-vis spectra of HNHCB (1×10−5 M) and HNHCB in presence of toothpaste
in aqueous acetonitrile solution and Naked-eye color change (inset).
Aq. CH3CNsolution
oftoothpaste
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Fig. S28 Color change of test paper containing HNHCB (10-4 M) in presence of different
anions
1 F- Oac- H2PO4-
Cl-- NO3--
Br--
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Table S1. Some useful data calculated from fluorescence decay behavior of HNHCB and
its complexes with Cu2+
Table S2. Some useful theoretical parameters of HNHCB and after complexation with
Cu2+
Environment г1b(ns) г2
b(ns) г3b(ns) α1 α2 α3 τav (ns) χ2
CH3CN-H2O 0.06695 0.66899 5.44898 0.73 0.24 0.019 0.32 1.003
Cu(II) 0.124558 0.68152 4.85526 0.87 0.10 0.012 0.34 0.998
Substrates C14-O36 C17-N19 C17…O18 C22…N21 N19-N21 O36-H37 O-Cu2+ N-Cu2+
1 1.377 1.387 1.219 1.286 1.350 0.966 - -1+Cu2+ 1.415 1.324 1.22 1.286 1.350 1.70 1.651
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Scheme S2. Plausable mechanism of color change of HNHCB in presence of F-