The mechanisms of a bifunctional fluorescent probe for detecting fluoride and sulfite based on excited-state intramolecular proton transfer and intramolecular charge transfer.

The mechanisms of 2-(Benzo[d]thiazol-2-yl)phenol-based bifunctional probe (HBT-FS) for detecting fluoride (F-) and sulfite (SO3 2-) based on excited-state intramolecular proton transfer (ESIPT) and intramolecular charge transfer (ICT) have been theoretically studied. Laplacian bond order of HBT-FS indicates that the F- ion cleaves the Si-O bond and then forms Compound 2 possessing a six-membered ring with a hydrogen bond. Potential energy curves and dynamic simulations confirm that ESIPT in Compound 2 occurs along with this hydrogen bond and forms a keto structure with an emission at 623 nm, which agrees with the observed experimental value (634 nm) after adding F-. Therefore, the fluorescence red-shift (from 498  to 634 nm) of HBT-FS observed in experiment after adding F- is caused by ESIPT. The SO3 2- ion is added to the C5 site of HBT-FS, which is confirmed by orbital-weighted dual descriptor, and then forms Compound 3 with fluorescence located at 404 nm. The experimentally measured fluorescence at 371 nm after adding SO3 2- is assigned to Compound 3. Charge transfer analyses indicate that the ICT extent of Compound 3 is relatively weak compared with that of HBT-FS because of the destruction of the conjugated structure by the addition reaction of SO3 2-, which induces the blue-shift of the fluorescence of HBT-FS from 498 to 371 nm. The different fluorescence responses make HBT-FS a fluorescent probe to discriminatorily detect F- and SO3 2-.

INTRODUCTION

Fluorescent probes have received increan class="Chemical">sing attention due to their high sensitivity, good selectivity, reliability, noninvasive, and real time detection. A variety of fluorescent probes have been developed to detect cations, anions, and biomolecules in vitro and in vivo. The different detection mechanisms have been revealed and the common detection strategy is to observe the changes in fluorescence intensity or fluorescence wavelength. Therefore, it is key to design a probe with the fluorescence signal showing obvious change after adding the analyte. Organic molecules with excited-state intramolecular proton transfer (ESIPT) process often exhibit different photophysical properties before and after proton transfer because ESIPT induces a tautomerization process from enol to keto form. In this tautomerization process, the change of geometric structure from enol to keto form induced by the transfer of protons along with hydrogen bonds usually causes the large Stokes shift in fluorescent, which has been excessively studied. This unique photophysical property makes compounds with ESIPT ideal materials for the design of fluorescent probes with many potential applications, such as luminescent materials, photostabilizers, laser dyes, and so on.

As one of the n class="Chemical">benzothiazole derivatives, 2-(Benzo[d]thiazol-2-yl)phenol (HBT) exhibits a typical ESIPT process and is recognized as an ideal fluorophore to design the ratiometric fluorescent probes. So far, many probes for different analytes have been designed and synthesized based on a core of HBT. Wu et al. used HBT as fluorophore to synthesize two ratiometric probes (named HBT-ratio-F1 and HBT-ratio-F2) for detecting fluoride ions. Wang and his co-workers constructed a novel HBT-based near-infrared fluorescent probe for the detection of bisulfite. Yang et al. developed a rhodol derivative that contains HBT as a ratiometric fluorescent probe for sulfite. These probes have only one recognition group, so they can detect one kind of analyte at a time. However, there is more than one species in the real sample, so it is necessary to develop a multifunctional probe that can distinguish two or more analytes at the same time. Lately, a HBT-based bifunctional ratiometric fluorescent probe 2–(4-(benzo[d]thiazol-2-yl)-3-((tertbutyldimethylsilyl)oxy)benzylidene)malononitrile (HBT-FS) has been designed and synthesized by Song and his co-workers for the discriminative detection of fluoride (F−) and sulfite (SO32–). HBT-FS has two sensing groups: (1) tert-butyldimethylsilyl ether moiety is sensitive to F− and (2) C-C double bond is sensitive to SO32–. The spectral responses of HBT-FS to F− and SO32– have been measured in the titration experiments, showing that F− and SO32– induced the red-shift and blue-shift of the fluorescence of HBT-FS, respectively. Song and his co-workers proposed that HBT-FS discriminatorily detect F− and SO32– by the combination of the ESIPT and intramolecular charge transfer (ICT) mechanisms. However, the proposed mechanisms lack theoretical verification. The ESIPT process needs to be further theoretically determined because the unique dual fluorescence feature of ESIPT was not observed in the experiment. In addition, the information of ICT cannot be provided through the experiment and needs to be analyzed by theory.

In this work, the theoretical cn class="Chemical">alculations by density functional theory (DFT) and time-dependent density functional theory (TD-DFT) are conducted to investigate photophysical properties before and after the addition of F− and SO32– and reveal the detection mechanisms of HBT-FS to F− and SO32–. Laplacian bond order (LBO) and orbital-weighted dual descriptor isosurface are calculated to determine the reaction sites of F− and SO32–. The possible geometric configurations of HBT-FS and the products (Compound 2 and Compound 3) in the ground (S0) state and the first excited (S1) state have been optimized, and the absorption and emission spectra are simulated based on these optimized structures. Moreover, the scanned potential energy curves and dynamic simulations of Compound 2 are performed to investigate the ESIPT reaction kinetics. The frontier molecular orbitals (FMOs) and the isosurface of C+ and C− functions are analyzed to explore the ICT properties.

COMPUTATIONAL DETAILS

In this work, the structures of n class="Disease">HBT-FS and its products in the S0 and S1 states are optimized with the DFT and TDDFT methods, respectively. In the optimization process, the structures are not constrained. The transition state is searched with the transition state theory. Frequency analyses confirm that these optimized configurations have no imaginary mode and the transition state has only one imaginary frequency, which is further ensured by the intrinsic reaction coordinate (IRC) calculation. For the above calculations, after testing a large number of functionals (see Table S1), the mPW1PW91 functional combined with TZVP basis set is adopted because of the consistency with the experimental result. Considering the experimental environment, acetonitrile (ACN) is chosen as the solvent by using the integral equation formalism variant of the polarizable continuum model (IEFPCM). The absorption and emission spectra are calculated based on the optimized structures. All calculations in this work are carried out by Gaussian 16 package and dynamic simulations are performed by using Newton-X interfaced with Gaussian. LBO and orbital-weighted dual descriptor as well as the isosurface of C+ and C− functions are analyzed by Multiwfn based on the outputs of Gaussian.

RESULTS AND DISCUSSION

Geometric structures

In order to investigate the sensing progress, the geometries on class="Chemical">f the fluorescent probe HBT-FS in the S0 and S1 states have been optimized at the mPW1PW91/TZVP theoretical level. As shown in Fig. 1, HBT-FS is based on a core of 2-(benzo[d]thiazol-2-yl)phenol (HBT) and has two sensing groups, which are the tert-butyldimethylsilyl moiety and the dicyanovinyl group, respectively. The tert-butyldimethylsilyl moiety for detecting F− masks the phenolic hydroxyl group into the ether group, which inhibits the proton transfer process. The dicyanovinyl group for recognizing SO32– is attached to the meta position of the phenolic hydroxyl group in HBT and acted as an electron-withdrawing group. It can be seen from Fig. 1 that the benzothiophene moiety in HBT-FS is not coplanar with the benzene ring, and the dihedral angles δ(C1-C2-C3-S) in the S0 and S1 states are 41.97° and −14.65°, respectively. The change of the dihedral angle δ(C1-C2-C3-S) from the S0 state to the S1 state indicates that the benzothiophene moiety is twisted and is more coplanar with the benzene ring in the S1 state. The bond length of C4-C5 double bond in the dicyanovinyl group changes from 1.358 Å in the S0 state to 1.400 Å in the S1 state, which is extended by 0.042 Å. After adding F−, the tert-butyldimethylsilyl ether bond is cleaved to form Compound 2, which is also shown in Fig. 1. In Compound 2, the phenolic hydroxyl group is restored and forms an intramolecular hydrogen bond O-H···N with the adjacent nitrogen atom. The bond lengths of O-H and H···N in the S0 state are 0.995 Å and 1.691 Å, respectively. Upon photo-excitation, the bond lengths of O-H and H···N changes to 1.008 and 1.644 Å, respectively. In addition, the bond angle of θ(O-H···N) is increased from 147.6° the S0 state to 148.8° in the S1 state. Based on the lengthening of the O-H bond length and the shortening of the H···N bond length as well as the increase of the bond angle of θ(O-H···N), it can be confirmed that the intramolecular hydrogen bond O-H···N is strengthened in the S1 state, which will provide a driving force for proton transfer. The dihedral angles δ(C1-C2-C3-S) in the S0 and S1 states are both 0°, indicating that Compound 2 has a planar structure. The C4–C5 double bond lengths of Compound 2 in the S0 and S1 states are the same as those of HBT-FS, respectively, which are both not changed. For Compound 3 displayed in Fig. 1, it is the product formed after the addition of SO32–. The dihedral angle δ(C1-C2-C3-S) in Compound 3 changes from –44.45° in the S0 state to 3.06° in the S1 state, which demonstrates that the mainframe HBT is more planar in the S1 state. However, the C4–C5 bond length becomes 1.561 Å in the S0 state, which is close to the length of C–C single bond. Thus, it can be confirmed that the C4–C5 double bond of the dicyanovinyl group is broken and that the conjugate system is interrupted by SO32–.

FIG. 1.

Optimized structures of the fluorescent probe HBT-FS and the corresponding reaction product Compound 2 and Compound 3 at the mPW1PW91/TZVP theoretical level. Blue: N; Light blue: H; Gray: C; Yellow: S; Red: O; Fuchsia: Si.

Optimized structures of the n class="Chemical">fluorescent probe HBT-FS and the corresponding reaction product Compound 2 and Compound 3 at the mPW1PW91/TZVP theoretical level. Blue: N; Light blue: H; Gray: C; Yellow: S; Red: O; Fuchsia: Si.

Reactive site

Laplacian bond order (LBO) is a newly defined bond order based on a scn class="Chemical">aled integral of the Laplacian of electron density negative parts in fuzzy overlap space, which can better identify bonding strength because of the direct correlation with the bond dissociation energy. LBO for all bonds of HBT-FS has been calculated by Multiwfn to determine the cleavage site of F−. As shown in Fig. 2(a), the calculated LBO of Si-O bond (0.198) is significantly smaller than that of other bonds, indicating that the bonding strength of Si-O bond is relatively weak. Therefore, the Si-O bond is a favorable cleavage site. In addition, the transition state and the Gibbs free energy barrier of the cleavage reaction are calculated. The searched transition state is verified by IRC (shown in Fig. S1) to be correct. The Gibbs free energy barrier of this reaction is 9.15 kcal/mol. This relatively small energy barrier further indicates that the reaction is prone to occur. For the addition reaction of SO32–, the orbital-weighted dual descriptor constructed from Fukui functions is calculated to predict the reactive site. The green and blue isosurfaces shown in Fig. 2(b) represent nucleophilic and electrophilic regions, respectively. In general, a site with a large green or blue isosurface has remarkable nucleophilicity or electrophilicity. It is noted that the green isosurfaces distributed on the C4 and C5 atoms of C4–C5 double bond are relatively large, confirming that the C4 and C5 atoms are susceptible to undergo nucleophilic attack. In order to quantitatively assess nucleophilicity of the C4 and C5 sites, the condensed local nucleophilicity indices are calculated based on conceptual density functional, which are 0.0218 and 0.0748, respectively. Therefore, the C5 site has high nucleophilicity and SO32– should be added to this site. The transition state is searched and found at the position where the C4–C5 double bond is broken and the C–S bond is formed, which is further confirmed by IRC calculations (shown in Fig. S2).

FIG. 2.

Laplacian bond order (LBO) for all bonds (a) and orbital-weighted dual descriptor isosurface of HBT-FS (b).

Laplacian bond order (LBO) for n class="Chemical">all bonds (a) and orbital-weighted dual descriptor isosurface of HBT-FS (b).

Proton transfer in Compound 2

In Compound 2, the six-membered n class="Chemical">hydrogen bond ring formed by the phenolic hydroxyl group and the adjacent nitrogen atom provides a possibility for the proton transfer. In order to verify whether proton transfer can occur, the potential energy curves of the S0 and S1 states are scanned as a function of the O-H bond length, which can provide the change of energy with bond length. As seen from Fig. 3, the energy of the S0 state increases with the extension of the O–H bond length, indicating that the proton transfer process in the S0 state is unlikely to occur. However, there is an energy barrier of 1.99 kcal/mol between the enol and keto form in the S1 state, which is quite small and can be easily overcome. Thus, the proton transfer process of Compound 2 occurs in the S1 state and then forms a stable keto structure at the O-H bond length of 1.808 Å.

FIG. 3.

The calculated potential energy curves of Compound 2 in the S0 and S1 states at the MPW1PW91/TZVP theoretical level.

The calculated potentin class="Chemical">al energy curves of Compound 2 in the S0 and S1 states at the MPW1PW91/TZVP theoretical level.

In order to reveal more details on class="Chemical">f proton transfer process, the dynamic simulations of Compound 2 are performed by using Newton-X interfaced with Gaussian program. The initial conditions for each trajectory are generated by a sampling procedure using a harmonic-oscillator Wigner distribution for each normal mode. Thirty-two trajectories as a representative set are simulated with a time step of 1 fs under an NVT ensemble at 300 K. The simulated time range is set to 300 fs, which is long enough to cover an ultrafast proton transfer process. In these classical dynamics simulations, results such as state character, energies, and internal coordinates can be described by statistical analysis. The time evolutions of energies and bond lengths are shown in Figs. 4(a) and 4(b). As seen from Fig. 4(a), no surface hopping between the S0 and S1 states exists, and the current state is located at the S1 state, indicating that proton transfer will occur in the S1 state. These analyses' results are consistent with that of the potential energy curve analysis. The proton transfer time is defined as the average time in which the distances of the O-H and N-H bonds become equal, that is, the time at the intersection in Fig. 4(b). It can be seen from Fig. 4(b) that the intersection between the two bonds of O-H and N-H indicates proton transfer time constant at 155 fs, which further confirms the occurrence of ESIPT.

FIG. 4.

The time evolution of energies (a) and bond lengths (b) in Compound 2.

Electronic spectra

The titration experiment shows that upon the addition on class="Chemical">f F−, the absorption peak at approximately 385 nm decreases gradually accompanying the appearance of two new peaks (approximately 400 and 350 nm). However, after the addition of SO32–, only one absorption peak at approximately 300 nm is found. In order to investigate the attribution of these absorption peaks, the six low-lying absorbing transitions of HBT-FS, Compound 2, and Compound 3 are calculated based on the optimized structures of the S0 state at the mPW1PW91/TZVP theoretical level. Only the singlet transitions with wavelengths >300 nm are listed in Table I and the calculated absorption spectra are displayed in Fig. 5. As seen from Table I, for HBT-FS, the absorption peak corresponding to the first singlet transition (S0→S1) is at 392 nm with the oscillator strength of 0.6358, which is in accord with the experimental value (385 nm). For Compound 2, there are two permitted singlet transitions (S0→S1 and S0→S3), which are at 419 and 352 nm, respectively. The calculated absorption peaks of Compound 2 coincide with the two peaks (400 and 350 nm) appearing after the addition of F−, which further confirms that Compound 2 is the product. The absorption peak of Compound 3 is calculated to be at 307 nm, which is consisted with the experimental data (300 nm). Therefore, the newly formed absorption peak after the addition of SO32– is attributed to Compound 3.

TABLE I.

The calculated electronic excitation energies (nm), corresponding oscillator strengths, and the corresponding compositions of the low-lying singlet excited states for HBT-FS, Compound 2, and Compound 3.

	Transition	λ (nm)	f a	Compositionb	CI (%)c
HBT-FS	S0→S1	392	0.6358	H→L	95.55%
	S0→S2	363	0.0066	H-1→L	98.48%
	S0→S3	345	0.2286	H-2→L	71.09%
	S0→S4	335	0.0111	H-3→L	73.23%
Compound 2	S0→S1	419	0.7075	H→L	96.42%
	S0→S2	359	0.0364	H-1→L	84.99%
	S0→S3	352	0.4659	H-2→L	81.57%
Compound 3	S0→S1	307	0.3983	H→L	68.62%

Oscillator strength.

H, HOMO (highest occupied molecular orbital) and L, LUMO (lowest unoccupied molecular orbital).

CI, Composition index.

FIG. 5.

The calculated absorption and fluorescence emission spectra of HBT-FS, Compound 2, and Compound 3 at the mPW1PW91/TZVP theoretical level.

The calculated electronic excitation energies (nm), corresponding oscillator strengths, and the corresponding compon class="Chemical">sitions of the low-lying singlet excited states for HBT-FS, Compound 2, and Compound 3.

The calculated absorption and n class="Chemical">fluorescence emission spectra of HBT-FS, Compound 2, and Compound 3 at the mPW1PW91/TZVP theoretical level.

The fluorescence peak changed with incrementn class="Chemical">al addition of F− and SO32– to the solution of HBT-FS. The fluorescence at 498 nm gradually declined with the increase in F− and a new emission peak at 634 nm appeared simultaneously. For the addition of SO32–, the emission peak shifted from 498 to 371 nm. To study the fluorescence properties of HBT-FS, Compound 2, and Compound 3, the emission energies are calculated based on the optimized structures in the S1 state. The corresponding calculation results are listed in Table II and the spectral curves are shown in Fig. 5. The calculated emission peak of HBT-FS is at 518 nm, which is in accordance with the experimental value (498 nm). For Compound 2, the S1→S0 emission energies of the enol and keto structures have been calculated, which are at 511 and 623 nm, respectively. The emission peak of the keto structure agrees with the emission peak at 634 nm appearing after the addition of F−. Therefore, the fluorescence peak at 634 nm measured in the experiment is emitted from the keto structure rather than the enol structure, which has a red-shift of 105 nm compared to that of HBT-FS. As for Compound 3, the calculated emission peak is at 404 nm, which is close to the emission peak (371 nm) appearing after the addition of SO32–. Thus, the experimentally measured fluorescence of 371 nm is assigned to Compound 3, which has a blue shift of 114 nm compared to that of HBT-FS.

TABLE II.

The calculated fluorescence emission band in ACN at the mPW1PW91/TZVP theoretical level and the experimental value.

	Form	Transition	λ (nm)	fa	Compositionb	CI (%)c	Exp. (nm)d
HBT-FS		S1→S0	518	1.1852	L→H	99.07%	498
Compound 2	enol	S1→S0	511	1.1569	L→H	98.97%
	keto	S1→S0	623	0.3117	L→H	99.83%	634
Compound 3		S1→S0	404	1.1071	L→H	98.51%	371

Oscillator strength.

L, LUMO (lowest unoccupied molecular orbital) and H, HOMO (highest occupied molecular orbital).

CI, Composition index.

The experimental value of the fluorescence peak.

The calculated n class="Chemical">fluorescence emission band in ACN at the mPW1PW91/TZVP theoretical level and the experimental value.

L, LUMO (lowest unoccupied molecular orbitn class="Chemical">al) and H, HOMO (highest occupied molecular orbital).

The experimentn class="Chemical">al value of the fluorescence peak.

Charge transfer

In order to study the properties of charge transfer and explain the spectral shifts induced by F− and SO32–, the frontier molecular orbitals involved in the absorption and emission of HBT-FS, Compound 2, and Compound 3 are shown in Fig. 6. It can be seen from Table I that the first singlet transitions (S0→S1) for all molecules involve only the electronic transitions from the highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO), which are all ππ*-type transitions. As seen from Fig. 6, for HOMO of HBT-FS, the electron density is mainly localized on the frame molecule HBT. While for LUMO, it is mainly distributed on the benzene ring and dicyanovinyl moiety. Therefore, charge transfer occurs in HBT-FS upon photo-excitation. For Compound 2, the charge transfer characteristic of the S0→S1 transition is similar to that of HBT-FS and the second permitted singlet transition (S0→S3) is dominated by the transition from HOMO-2 to LUMO, which also has a ππ* feature. For Compound 3, the first singlet transition (S0→S1) corresponding to the transition from HOMO to LUMO involves a charge transition process from HBT to dicyanovinyl moiety. As for the emission of HBT-FS, Compound 2, and Compound 3, the S1→S0 transitions are all corresponding to the electronic falling from LUMO to HOMO. It can be noted that the electron density on dicyanovinyl moiety in HBT-FS and Compound 2 decreases and ICT in Compound 3 mainly occurs on the frame molecule HBT due to the destruction of the conjugated structure by the addition reaction of SO32–. For Compound 2, it can be noted that the energy gap of keto structure (2.66 eV) from LUMO to HOMO is smaller than that of enol structure (3.55 eV), indicating that keto form structure will emit long-wavelength fluorescence. Thus, the red-shift of fluorescence after adding F− is caused by ESIPT. For Compound 3, the energy gap (3.82 eV) from LUMO to HOMO increases compared to that of HBT-FS (3.02 eV), which will emit relatively short-wavelength fluorescence.

FIG. 6.

Frontier molecular orbitals involved in the vertical excitation and emission of HBT-FS, Compound 2, and Compound 3.

Frontier molecular orbitn class="Chemical">als involved in the vertical excitation and emission of HBT-FS, Compound 2, and Compound 3.

In order to compare the ICT characteristics between the S0 and S1 states quantitatively, the electron density din class="Chemical">fferences in the S0 and S1 structures are calculated for HBT-FS, Compound 2, and Compound 3. Figure 7(a) shows the electron density difference in the S0 structure during the electron excitation. The green and blue regions correspond to positive and negative regions, respectively, which represent the increase and decrease in electron density in the electron excitation process. It can be noted that the increase in electron density is mainly in dicyanovinyl moiety, which is consistent with the results of FMOs analysis. In order to visualize the characteristics of charge transfer more intuitively, the isosurfaces C+ and C- functions are shown in Fig. 7(b). C+ and C− functions proposed by Bahers et al. represent two centroids of charges associated with the positive and negative density regions, respectively, which make the direction of electron transfer clearly visible. In addition, the distance between the barycenters of C+ and C- can be used to measure the charge-transfer length to evaluate the charge-transfer degree. In general, the longer the charge-transfer length, the greater the charge-transfer degree. It can be seen from Fig. 7(b) that the charge-transfer lengths between the barycenters of C+ and C− in HBT-FS, Compound 2, and Compound 3 are 4.514, 3.968, and 1.072 Å, respectively. Therefore, compared to HBT-FS and Compound 2, Compound 3 has the smaller charge transfer distance, indicating that Compound 3 has a smaller extent of charge transfer characteristic corresponding to the S0→S1 transition. In addition, the dipole moment variations from the S0 state to the S1 state for HBT-FS and Compound 2, Compound 3 are 11.30 D, 14.75 D, and 3.19 D, respectively. The insignificant dipole moment variation of Compound 3 further illustrates a weak ICT characteristic in Compound 3.

FIG. 7.

The electron density difference between the S0 and S1 states in the S0 structure (a) and in the S1 structure (c). The isosurface of C+ (green) and C− (blue) functions as well as the charge-transfer distances for HBT-FS, Compound 2, and Compound 3 in the S0 structure (b) and in the S1 structure (d).

The electron density din class="Chemical">fference between the S0 and S1 states in the S0 structure (a) and in the S1 structure (c). The isosurface of C+ (green) and C− (blue) functions as well as the charge-transfer distances for HBT-FS, Compound 2, and Compound 3 in the S0 structure (b) and in the S1 structure (d).

Figures 7(c) and 7(d) show the electron denn class="Chemical">sity differences and the isosurface of C+ and C- functions based on the S1 structures in the electron de-excitation process, respectively. It can be noted that the charge-transfer lengths for all molecules vary as the structures transfer from the S0 state to the S1 state. The ICT distances corresponding to the S1→S0 transition of HBT-FS, Compound 2, and Compound 3 become 3.991, 3.956, and 1.301 Å, respectively. The ICT distance in Compound 3 is still the smaller one compared to that in HBT-FS and Compound 2, confirming a smaller ICT extent. Thus, the addition reaction of SO32– weakens the ICT extent, which leads to the blue-shift (from 498 to 371 nm) of the fluorescence of HBT-FS. In addition, it can be seen that the ICT distances of HBT-FS and Compound 3 change relatively obviously compared to that of Compound 2. This is because the molecular structures of HBT-FS and Compound 3 undergo rearrangement, which has been confirmed by the changes of dihedral angles δ(C1-C2-C3-S) from the S0 state to the S1 state.

Detection mechanisms

According to the previous spectral measurements and the current theoreticn class="Chemical">al calculations, the fluorescent probe HBT-FS exhibits different fluorescence responses to F− and SO32–. Based on the correlation analyses, the detection mechanisms of HBT-FS for F− and SO32– can be plotted as in Fig. 8. HBT-FS with the tert-butyldimethylsilyl moiety and the dicyanovinyl group as sensing groups shows an emission peak at 498 nm. The addition of F− cleaves the tert-butyldimethylsilyl ether bond in HBT-FS to form Compound 2 with a six-membered hydrogen bond ring. Upon photo-excitation, an ESIPT process in Compound 2 occurs along the hydrogen bond to form a keto structure with an emission at 623 nm, which is red-shifted compared to the emission peak of HBT-FS. For the addition of SO32–, it will be added to the C5 site of the C4–C5 double bond in HBT-FS to form a Compound 3 with an emission at 371 nm. The addition reaction of SO32– breaks the conjugate structure of HBT-FS and weakens the intramolecular charge transition, thereby inducing the fluorescence blue-shift of HBT-FS from 498 to 371 nm. Based on the different fluorescence behaviors induced by the addition of F− and SO32–, HBT-FS can act as a fluorescent probe to discriminatorily detect F− and SO32–.

FIG. 8.

The schematic diagram of fluorescence response mechanisms of HBT-FS for F− and SO32–. RGSIPT: Reverse ground state intramolecular proton transfer.

The schematic diagram of n class="Chemical">fluorescence response mechanisms of HBT-FS for F− and SO32–. RGSIPT: Reverse ground state intramolecular proton transfer.

CONCLUSIONS

In this work, the DFT and TDDn class="Chemical">FT calculations have been performed to investigate the detection mechanisms of 2-(benzo[d]thiazol-2-yl)phenol-based bifunctional probe (HBT-FS) for F− and SO32–. LBO confirms that Si-O bond in HBT-FS is easily cleaved by F− due to a smaller LBO (0.198) and then forms Compound 2 with a six-membered hydrogen bond ring. The constructed potential energy curves and dynamic simulations demonstrate that the ESIPT process in Compound 2 occurs along this hydrogen bond to form a keto structure with an emission at 623 nm, which is consistent with the observed experimental value (634 nm). Therefore, the red-shift of the fluorescence of HBT-FS from 498 to 634 nm after adding F− is caused by ESIPT. For SO32–, orbital-weighted dual descriptor isosurface verifies that it is added to the C5 site of HBT-FS and then forms Compound 3, which emits fluorescence at 404 nm. Thus, the experimentally measured fluorescence at 371 nm is assigned to Compound 3. In order to explain the blue-shift of the fluorescence of HBT-FS from 498 to 371 nm after adding SO32–, ICT is analyzed by frontier molecular orbitals and the isosurface of C+ and C− functions. The analysis results demonstrate that ICT extent in Compound 3 is relatively weak compared with that in HBT-FS because of the destruction of the conjugated structure by the addition reaction of SO32–, which results in the blue shift of fluorescence of HBT-FS. These different fluorescence responses make HBT-FS a fluorescent probe to discriminatorily detect F− and SO32–.

See the supplementary material n class="Chemical">for some functionals test results and IRC calculations.