Orientation of 2,6-Dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide on Silver Nanoparticles: Surface-Enhanced Raman Spectral Studies

Anuratha, M.; Jawahar, A.; Umadevi, M.; Edayadulla, N.; Sathe, V. G.; Meenakumari, V.; Milton Franklin Benial, A.

doi:https://doi.org/10.1155/2014/175023

International Journal of Spectroscopy

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Abstract Introduction Experimental Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2014 | Article ID 175023 | https://doi.org/10.1155/2014/175023

Orientation of 2,6-Dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide on Silver Nanoparticles: Surface-Enhanced Raman Spectral Studies

M. Anuratha,¹A. Jawahar,²M. Umadevi,³N. Edayadulla,⁴V. G. Sathe,⁵V. Meenakumari,⁶and A. Milton Franklin Benial⁶

Academic Editor: Jin Zhang

Received22 Oct 2013

Accepted13 Dec 2013

Published06 Feb 2014

Abstract

Silver nanoparticles were synthesized using solution combustion method with citric acid as fuel. The prepared silver nanoparticles exhibit fcc crystalline structure with particle size of ~50 nm. The morphology and purity of the silver nanoparticles were also studied by high-resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX). Surface-enhanced Raman scattering (SERS) spectra of 2,6-dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide (DBTD) adsorbed on silver nanoparticles were investigated. Orientation of DBTD on silver nanoparticles has been inferred from normal Raman spectrum (nRs) and SERS spectral feature. The observed spectral feature evidenced that DBTD would adsorb on silver surface with tilted orientation through the lone pair electrons of C–N, C=O, S=O, and pyridine ring. The present investigation has been a model system to deduce the interaction of drugs with DNA.

1. Introduction

Surface-Enhanced Raman spectroscopy (SERS) is a Raman spectroscopic (RS) technique that provides enhanced Raman signal from Raman-active molecules that have been adsorbed onto certain specially prepared metal surfaces. Increases in the intensity of Raman signal have been regularly observed in the order of 10⁴–10⁶ and can be as high as 10⁸ and 10¹⁴ for some systems [1, 2]. The discovery of such an enormous enhancement in the Raman intensity when a molecule is in the vicinity of metal nanoparticles, coupled with the suppression of fluorescence, generated considerable excitement and suggested the possibility that SERS could provide an invaluable tool as a reliable, high-resolution detection technique for extremely minute quantities of target molecules [3].

SERS selectivity of surface signal results from the presence of surface-enhancement mechanisms only at the surface. SERS completely overcomes the disadvantage of the small cross-section of Raman spectroscopy and could be used to study the single molecule spectroscopy [4]. The structural and molecular identification power of RS can be used for numerous interfacial systems, including electrochemical, modeled, and actual biological systems; catalytic, in situ, and ambient analyses, and other adsorbate-surface interactions [1, 5]. Due to the sensitivity of SERS, detection of trace molecules can be made [6]. SERS is observed primarily for analytes adsorbed onto coinage or alkali metal surfaces, with the excitation wavelength near or in the visible region [7]. The symmetry of a molecule can be changed in different ways depending on the orientation in which the molecule is attached to the surface. In some experiments, it is possible to determine the orientation of adsorption to the surface from the SERS spectrum, as different modes will be present depending on how the symmetry is modified [8]. It is highly desirable to apply in situ SERS to obtain molecular level information about the breaking and formation of bonds in the reaction, observe the reaction intermediate on the surface, and finally distinguish the reaction products [9].

Heterocycles containing nitrogen and sulfur possess important biological activities. Thiazines are six-membered heterocycle containing one sulfur atom and one nitrogen atom. A number of isomeric structures are possible depending upon the relative positions of the two hetero atoms and the degree of oxidation of the ring system. Thiazines display many important biological activities such as antitussive [10], anesthetic [11], antiradiation [12], anticonvulsant [13], sedative [14], anticoagulant [15], neuroleptic [16], and herbicide antidote [17]. They have been used as cardiovascular agents [15], antihypertensive [16], antiviral [17], anti-HIV [18], antifungal [19], anti-inflammatory [19], anthelmintic [19], and antipsoriatic [20]. The thiazine derivatives should be subjected to close scrutiny for biological action. In recent times, the cephalosporins have been used as antibiotics of great value. These mould metabolites, which contain a fused β-lactam-dihydro-1,3-thiazine skeleton, are obviously related to the penicillins and their discovery has initiated a major study which is still in progress to optimize their therapeutic effects. Earlier, tetrahydro-1,4-thiazine-1-oxide-3-carboxylic acid was isolated from algae, and recently, tetrahydro-1,4-thiazine-3,5-dicarboxylic acid has been detected in the bovine brain and human urine [21, 22].

The adsorption of biomolecules on metal substrates has been a subject of great interest for researchers due to its broad potential applications. SERS has become a valuable tool for monitoring the changes in the chemical nature of the molecule adsorbed on metal surface. In this work, the effect of silver nanoparticles on the enhancement of SERS spectra and orientation of DBTD on the prepared silver nanoparticles was investigated. The present investigation has been a model system to deduce the interaction of drugs with DNA.

2. Experimental

2.1. Reagents

Silver nitrate, citric acid, diethyl 2,2′-sulfonyldiacetate, pyridine-3 carboxaldehyde, and ammonium acetate were obtained from Sigma Aldrich Chemical and was used without further purifications. All glasswares were properly washed with distilled water and dried in hot air oven before use.

2.2. Preparation of Silver Nanoparticles

Stoichiometric amount of silver nitrate (1.6987 g) was dissolved in deionised water (10 mL) and then citric acid (0.277 g) was added into it. The solution was kept in the furnace at 300°C. With large amount of fumes, the combustion reaction was completed in 15 mins and loose powder was formed. This was crushed and ground thoroughly.

2.3. Preparation of 2,6-Dicarbethoxy-3,5-bis(pyridine-3-yl) tetrahydro-1,4-thiazine1,1-dioxide

To an alcoholic solution (50 mL) of diethyl 2,2′-sulfonyldiacetate (0.01 M), pyridine-3 carboxyaldehyde (0.02 M) and ammonium acetate (0.02 M) were added and the mixture was refluxed for 2 hr. The reaction mixture was concentrated to half of its original volume and allowed to cool in an ice chest. The solid that separated was filtered, washed with ice cold aqueous ethanol, and crystallized from petroleum ether (60–80°C): chloroform (1 : 1). Figure 1 shows the structure of 2,6-dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide.

2.4. Experimental Techniques

The silver nanopowders were subjected to X-ray diffraction analysis (PANalytical X’pert—PRO diffractometer system, Eindhoven, The Netherlands) and target was Cu Kα with a wavelength of 1.5406 Å. The generator was operated at 40 kv and with a 30 mA current. The scanning range was selected between 10° and 100°. The size, composition, and atomic structure of the NPs were analyzed by high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX) using a 200 kV JEOL JEM 2100 microscope with lattice resolution of 0.14 nm and point-to-point resolution of 0.19 nm. The samples were made by depositing the Ag NPs on a carbon coated Cu grid and the size measurements were performed manually on HRTEM images. The Raman spectra were recorded in the wavelength region 400–1100 nm by micro-Raman system (Jobin Yvon Horiba LABRAM-HR visible) using He–Ne as excitation laser source at wavelength 632.8 nm. Using confocal optics a lateral resolution of 1 micron and an axial resolution of 2 micron can be achieved. 600 and 1800 lines/mm gratings were used for dispersive geometry, the charge-coupled device (CCD) camera was used as the detector with the spectral resolution of 1 cm⁻¹.

3. Results and Discussion

3.1. XRD and HRTEM Studies

The XRD pattern of prepared Ag nanoparticles was compared and interpreted with standard data (JCPDS ICDD 04-0783). In the XRD pattern (Figure 2), four diffraction peaks were observed at , , , and which correspond to (1 1 1), (2 0 0), (2 2 0), and (3 1 1) Bragg’s reflections of the face centered cubic (fcc) structure of metallic silver, respectively. The peak line width in the XRD spectra is broadened due to smaller particle sizes. This XRD line width can be used to estimate the size of the particle by using the Debye-Scherrer formula as where is the particle size, is the wavelength of X-ray radiation (1.5406 Å), is the full width at half maximum (FWHM) of the peak (in radians) and is the Bragg angle. The calculated average particle size is found to be ~50 nm. The lattice constant values were also calculated and they agree well with the standard data. The sample exhibits smaller cell volumes than that of bulk.

HRTEM is a high-spatial-resolution structural and chemical characterization tool and provides exact information about particle size and shape. Figure 3(a) shows the HRTEM image of the preparation of the prepared silver nanoparticles. Figure 3(b) shows the energy dispersive X-ray analysis spectrum (EDX) of the prepared silver nanoparticles. It confirms the presence of elemental silver signal. The silver nanocrystallites display an optical absorption band peak at approximately 3 eV, which is due to surface plasmon resonance. The signal of Cu originated from the copper grid.

(a)

(b)

3.2. SERS Studies

3.2.1. Vibrational Assignments

Figure 4 shows the normal Raman spectrum (nRs) of DBTD. Figure 5 depicts the SERS spectrum of DBTD in silver nanoparticles. Table 1 shows the vibrational modes and its corresponding assignments.

(a)

(b)

(a)

(b)

NH stretching vibration generally occurs in the region 3300–3500 cm⁻¹ [23]. The peak observed at 3275 cm⁻¹ in nRs is assigned to NH stretching vibration. In the Raman spectrum of monosubstituted benzene, the bands which appear in the region 3000–3100 cm⁻¹ are due to aromatic CH stretching vibrational mode [23]. In the present compound, the band observed at 3069 cm⁻¹ in nRs is assigned to the CH stretching mode. In an aliphatic compound, the asymmetric and symmetric CH stretching mode of methylene group occur near 2960 and 2870 cm⁻¹, respectively [23]. In nRs,the symmetric CH stretching mode observed at 2878 cm⁻¹ is attributed to the symmetric CH stretching mode and the asymmetric CH stretching mode of methylene appeared at 2967 cm⁻¹.

The carbonyl stretching mode falls in the region 1700–1685 cm⁻¹ for ketones [23]. In the present case, the band observed at 1724 and 1674 cm⁻¹ is due to C=O stretching mode. Generally C–C stretching mode is observed around 1602 cm⁻¹ [23]. In the case of pyridine the C–C and C–N stretching modes are observed in the region 1430–1603 cm⁻¹ [24]. In the case of phenothiazine, the ring stretching mode is observed in the region 1570–1605 cm⁻¹ [25]. In DBTD, the modes observed in the region 1610–1420 cm⁻¹ are assigned to C–C stretching and C–N stretching of pyridine. The asymmetric S=O stretching mode of thiazine dioxide is observed at 1350 and 1368 cm⁻¹ [26]. The asymmetric SO₂ and symmetric SO₂ stretching modes are observed at 1321 and 1281 cm⁻¹, respectively [23]. In the present case, these modes are observed at 1323 and 1283 cm⁻¹ in nRs and 1304 and 1270 cm⁻¹ in SERS, respectively. In phenothiazine symmetric Ph–N–Ph stretching mode is observed at 1250 cm⁻¹ [27]. In the present case the modes observed at 1225 cm⁻¹ in nRs and 1254 cm⁻¹ in SERS are due to Ph–N–Ph stretching mode. The vibrational modes occuring at 1204 and 1185 cm⁻¹ are assigned to CH in-plane bending mode. The symmetric S=O stretching mode is observed at 1130 cm⁻¹ in nRs and 1140 cm⁻¹ in SERS [26]. The vibrational mode observed at 1110 cm⁻¹ is due to asymmetric C–N–C stretching. The bands at 1041, 1030, 1028, 982, 902, and 901 cm⁻¹ are due to ring breathing vibrations. In nRs, the symmetric C–N–C stretching mode and Ph–S–Ph stretching mode are observed at 841 and 671 cm⁻¹ respectively. In SERS, the vibrational modes observed at 860 and 877 cm⁻¹ are assigned to symmetric C–N–C stretching mode and another mode observed at 695 cm⁻¹ is due to Ph–S–Ph stretching mode. In SERS, the CH out-of-plane bending is observed at 722 cm⁻¹. In pyridine, the in-plane ring deformation is observed at 603 cm⁻¹ [24]. In the present case, the in-plane ring deformation modes are observed at 634 and 610 cm⁻¹ in nRs. In SERS, the in-plane ring deformation mode is observed at 591 cm⁻¹. In the present case, OSO bending mode is observed at 526 cm⁻¹ in nRs and 547 cm⁻¹ in SERS. This mode occurs at 514 cm⁻¹ in phenothiazine. The out-of-plane ring deformation modes are observed at 491 and 420 cm⁻¹ in nRs and the corresponding modes appeared at 503 and 409 cm⁻¹, respectively, in SERS.

3.2.2. Orientation Studies

There are two main mechanisms which are responsible for the observed enhancement and the shift in the SERS. One is the long range electromagnetic mechanism and the other one is the short range chemical enhancement mechanism. The electromagnetic mechanism is based on the amplification of the electromagnetic field generated due to the coupling of the radiation field with the surface plasmons of metal nanoparticles. It depends on the optical properties of the nanostructured substrate. The chemical enhancement mechanism is based on the charge transfer between the metal surface and the adsorbed molecule [28, 29]. It may be from the HOMO of the molecule to the Fermi level of the metal or from the Fermi level of metal to the LUMO of the molecules. This mechanism depends on the chemical nature of the adsorbed molecules.

The surface-enhancement depends on the following factors. The first effect is the kind of adsorption between chemical compounds and metal NPs, that is, chemisorption or physisorption. Chemisorption shows high surface-enhancement when compared to physisorption. The second effect depends on the orientation of the chemical compound on the metal NPs, that is, flat-on or stand-on orientation. The third effect involves the polar substitute of the chemical compound, which indicates the electron withdrawing or donating groups [30].

The orientation/adsorption mechanism of a DBTD can be deduced from its SERS spectrum through a detailed analysis of the peak shift and band broadening caused by the surface adsorption [31]. The DBTD molecule has different binding sites such as pyridine ring, lone pair electrons of oxygen, and lone pair electrons of nitrogen. There are three possible orientations that the molecule may adsorb on metal surfaces such as face-on, tilted, and stand-on orientations. The SERS effect is stronger in molecules with electron lone pairs and also in molecules with electron density. The orientation of the adsorbed molecule on the metal surface can be inferred from the intensity variation and shift in vibrational wavenumber of the modes in SERS with respect to the corresponding modes in nRs.

These binding sites may lead to the adsorption of the molecule on the silver surface. The orientation of DBTD on the silver surface can be inferred from the aromatic CH stretching vibrations, ring stretching/breathing vibrations, in-plane and out-of-plane vibrations, and surface selection rules. According to the SERS investigation of benzene derivatives, the ring modes have to redshift by around 10 cm⁻¹ along with an increase in their bandwidth. It shows that the surface-ring orbital interaction is the driving force of the surface adsorption. The red shift can be attributed to the bond weakening caused by the electron back donation from the metal to the antibonding orbital of the benzene moiety [32].

When a molecule is adsorbed flat-on the silver surface, its out-of-plane bending modes will be more enhanced compared to its in-plane bending modes according to surface selection rule and vice versa when a molecule is adsorbed perpendicular to the surface [33]. Another possible way in which the DBTD derivative stand-on adsorption occurs on the silver surface is through the C=O. The most intense signals were obtained for oxygen containing compounds bearing electron systems. Carboxylate and ester groups can interact strongly with metal through the formation of CT complexes between adsorbate and metal NPs where adsorbate acts like a donor and the metal like an acceptor [34]. The carbonyl oxygen makes a good binding site for surface adsorption over the metal surface. When the carbonyl groups are chelated to the metal surface, the wavenumber of the C=O stretching mode is decreased [35]. In the present case, a single band is observed at 1719 cm⁻¹ in nRs of DBTD due to C=O stretching mode.

In this work, DBTD can interact with silver surface through the lone pairs of the oxygen atom of the C=O group. According to the surface selection rule when DBTD is adsorbed on silver surface through lone pair electron of oxygen atom of the C=O group, these modes should be appeared as prominent modes with high intensity because the polarizability tensor component is normal to the silver surface. In the present case, this prominent mode is observed at 1724 cm⁻¹ in SERS, which indicates that the adsorption of the DBTD molecule on silver nanoparticles is through C=O group.

Most of the bands are broadened in SERS. Generally, SERS bands of adsorbate undergo band broadening. The homogeneous and inhomogeneous contributions are responsible for the observed broadening of peaks in SERS. The homogeneous effect arises due to fundamental intramolecular interactions that will affect the lifetime and dephasing of vibrations in molecules. The inhomogeneous effect originates from the external perturbations which resulted in changes in the frequency and full width at half-maximum (FWHM) value of individual molecules. When the molecule approaches a metal surface, the electrons present in its levels undergo tunneling between the molecule and the metal. Consequently, the metal gives it a finite lifetime and hence larger FWHM [36].

Analysis of spectral line shape can provide information on vibrational dynamics, such as vibrational dephasing, which may occur by a pure dephasing and/or by energy relaxation. In pure dephasing relaxation, dynamic fluctuations of the oscillator frequency destroy the phase relationship. Energy relaxation results from the change of the oscillator phase during the energy exchange which occurs in the process of the depopulation of vibrational states. Since both the frequency fluctuations and energy relaxation are due to intra- and intermolecular interactions of the oscillator with the surrounding molecules, the dephasing provides information about the dynamics of interactions and molecular motions around the oscillator [37].

The SERS spectral investigations show the prominent peaks at 1610, 1537, 1368, and 1028 cm⁻¹. The SERS bands observed at 1610 and 1537 cm⁻¹ are shifted by 19 and 40 cm⁻¹, respectively. The red shift may be due to the C=N bond weakening caused by the electron back donation from metal to the antibonding orbital of the C=N bond. The blue shift was explained by invoking the fact that the lone pair electrons have antibonding character and the electron donation to the silver surface may increase the strength of the CN bond [38].

This blue shift can be explained by considering that the interaction of the pyridine with the metal takes place via the electron of C=N bond as well as the lone pair electrons of nitrogen. The blue shift can also be caused by an increase in the force constant of the corresponding vibrational mode. It may also be due to the electron charge from the molecule to the metal surface due to adsorption. The blue shift can be explained in terms of a repulsion interaction between DBTD molecules, which are present in different charge states. This may decrease the bond length and lead to blue shift [39].

The FWHM values of these modes increase due to adsorption. The observed high FWHM value may be due to the decrease in vibrational relaxation time of the DBTD on the metal surface. It also gives the evidence that the molecules (DBTD) are oriented in different form in the silver surface. The larger FWHM values reflect inhomogeneous band broadening associated with strong interactions between pyridine ring and silver surface.

The observed downshifted ring breathing mode in SERS observed at 1028 cm⁻¹ shows that there may be weakening of the bonds in the pyridine ring system caused by electron donation from pyridine ring to silver surface or electron back donation from silver surface to pyridine ring. But the intensity of this band is decreased in SERS. Therefore the orientation of DBTD on silver surface cannot be deduced from this ring breathing vibrations. The ring stretching vibration (C–C) of DBTD is observed at 1610 and 1537 cm⁻¹ are shifted by 19 and 40 cm⁻¹, respectively. The band width of these bands increases. These spectral changes in ring stretching vibration indicate that the DBTD molecules adsorb on the metal surface via their system [32].

In the present case the in-plane and out-of-plane vibrations observed in nRs have no counterpart in SERS. Therefore the orientation determination from in-plane and out-of-plane vibrations will be neglected. The adsorption of different charge state of DBTD on silver surface may give rise to orientation effects which essentially change the symmetry of the adsorbed DBTD. As the result, the mode which is inactive in nRs becomes active in SERS, which gives rise to the bands at 877 and 982 cm⁻¹ in SERS due to symmetric C–N–C stretching and ring breathing mode, respectively. The intense SERS band at 1368 cm⁻¹ is due to asymmetric S=O stretching mode.

SERS selection rules which can be inferred from both charge transfer and electromagnetic mechanisms consider that vibrations with polarizability tensor normal to the surface suffer the highest intensity enhancement, since these vibrations imply electronic displacements which interact with the electromagnetic field produced by the surface plasmons [40]. According to this, those bands which increase in intensity give insight on the orientation of the molecule into the surface. In the present case, the DBTD molecule can be anchored on the silver surface through lone pair electron of S=O. As a result the polarizability tensor of this mode will be normal to the surface. According to the charge transfer and electromagnetic mechanism this vibrational mode gets enhanced intensity. The presence/absence of the benzene ring CH stretching vibration is a reliable probe for the perpendicular/parallel orientation, respectively, of the benzene ring with respect to the surface [37, 41]. In the present case, the ring CH stretching band is present in nRs which is absent in the SERS. This means that the DBTD may be adsorbed flat-on orientation on the silver surface. The observed spectral feature evidenced that DBTD would adsorb on silver surface with tilted orientation through the lone pair electrons of C–N, S=O, and pyridine ring.

4. Conclusion

The orientation of 2,6-dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide (DBTD) adsorbed on silver nanoparticles was studied using SERS. Silver nanoparticles were synthesized using a solution combustion method with citric acid as fuel. The prepared silver nanoparticles have an FCC crystalline structure with the particle size of ~50 nm. The nRs and SERS spectral analysis reveals that the DBTD adsorbed tilted (neither flat-on nor stand-on) orientation on the silver surface. The morphology and purity of the silver nanoparticles were also studied by HRTEM and EDX techniques.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors M. Anuratha, A. Milton Franklin Benial, A. Jawahar, and V. Meenakumari thank their college management for encouragement and permission to carry out this work. One of the authors, M. Umadevi, is thankful to UGC-DAE-CSR, Indore, and DST-CURIE and DST-SERB, New Delhi, for financial assistance.

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Copyright © 2014 M. Anuratha et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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