Synthesis, Characterization, and DNA-Binding Kinetics of New Pd(II) and Pt(II) Thiosemicarbazone Complexes: Spectral, Structural, and Anticancer Evaluation

In a bid to come up with potential anticancer agents, a class of thiosemicarbazone ligands bearing substituted thiophene were synthesized followed by complexation with various Pd(II) and Pt(II) metal precursors. 'e ligands (E)-1-((thiophen-2-yl) methylene)thiosemicarbazide (L1), (E)-1-((4-bromothiophen-2-yl)methylene)thiosemicarbazide (L2), and (E)-1-((5-bromothiophen-2-yl)methylene)thiosemicarbazide (L3) were synthesized by condensation reactions and obtained in good yields. Complexation of L1 and L2 with Pd(cod)Cl2 gave C1 (C6H7Cl2N3PdS2) and C2 (C6H6BrCl2N3PdS2), respectively. Complexation of L1 with K2PtCl4 gave C3 (C6H7Cl2N3PtS2), while L3 with K2PtCl2[(PPh)3]2 gave C4 (C24H21BrClN3PPtS2). 'e structures and coordination for all compounds were established by FTIR, H-NMR, C-NMR, UV-Vis, elemental analysis, and single-crystal X-ray diffraction studies for ligand L1. Tuning of the spectral and anticancer activity of the compounds was investigated by changing the position of the bromide substituent, metal center, and the σ or π-donor/acceptor strength of the groups surrounding the metal center.'e compounds had low to moderate anticancer potency with their spectral and structural properties correlating with the corresponding anticancer activity profiles. DNA binding modes were studied by spectroscopy and were comparable to known DNA intercalators. Structure-activity profiles were evident especially between C1 and C2 differing by the presence of a Br in position 5 of thiophene ring, which caused a remarkable increase in IC50 values, from 14.71± 0.016 (C1) to 43.08± 0.001(C2) in Caco-2 cells, 1.973± 0.048 (C1) to 59.56± 0.010 (C2) in MCF-7 cells, 16.65± 0.051 (C1) to 72.25± 0.003 (C2) in HeLa cells, 14.64± 0.037 (C1) to 94.34± 0.003 (C2) in HepG2, and 14.05± 0.042 (C1) to >100(C2) in PC-3 cells.


Introduction
Cancer is the second leading cause of death globally, with an estimated 1 in 6 deaths, and is responsible for an estimated 9.6 million deaths in 2018 [1]. It is estimated that approximately 70% of all deaths are cancer-related and occur in low-and middle-income countries [1]. e economic impact of cancer is significant and is increasing with a total annual economic cost of cancer in 2010 estimated at approximately US$ 1.16 trillion. Only 1 in 5 low-and middle-income countries have the necessary data to drive cancer policy [1]. Although major steps have been made in medicine, many difficulties still need to be resolved in order to boost cancer therapy. In line with this, research is putting a great deal of effort into discovering new and effective therapeutics that can mitigate the pertinent adverse effects. Many research reports have focused on creating alternative treatments to minimize the side effects of traditional medicines over the past decade [2][3][4]. e most practiced efforts to combat cancer include surgery, chemotherapy using chemical drugs, and radiotherapy using electromagnetic radiation like X-rays to kill cancerous cells. New strategies like gene therapy are still being developed where genes from donors are inserted into the DNA of a patient to boost recognition of cancerous cells by the body's diseases fighting mechanisms. Some of the most successful chemotherapeutic drugs include those derived from metals like platinum, ruthenium, titanium, and palladium, among others.
Research on thiosemicarbazone compounds for medical applications appeared as early as 1950s when they were used against TB and leprosy [5]. e following decade saw these compounds tested for antiviral properties which were confirmed, leading to intense research which eventually culminated to the commercialization of some thiosemicarbazone products under trade names methisazone and Marboran ® , in the treatment of smallpox [6]. Another major step in utilization of these compounds was the publication of the first antitumor tests [7]. Finch and coworkers explored the broad areas of application where thiosemicarbazones have received most attention, classifying them in relation to their activities against cancerous cells, protozoa, bacteria, or viruses. eir activity is found to correlate to the type of metal center [8]. As anticancer agents, the activity is shown to substantially increase for the complexed product as compared to the free ligand, and also, the undesirable cytotoxicity as side effects was shown to be minimized in the complexes [8].
is work reports the anticancer activity of newly synthesized Pd(II) and Pt(II) complexes bearing thiosemicarbazone ligands. e main objectives were to evaluate the tuning of structure-activity relationships vis-à-vis different σ and/or π-donor/acceptor properties of the groups attached to the metal center, their anticancer activities, and their binding modes to DNA.
Anticancer and apoptotic properties were performed in vitro using human colon (Caco-2), human cervical (HeLa), human hepatocellular carcinoma (HepG2), breast cancer (MCF-7), human prostate (PC-3), and noncancer human breast (MCF-12A) cells. Binding modes to DNA were studied by use of calf thymus DNA (CT-DNA). A crystal structure of one of the ligands, L1, is also reported here for the first time according to the CCCD database.

Materials and Methods
All synthetic manipulations were performed under the fume hood under inert conditions. e solvents were of analytical grade, and each was dried with the recommended drying agent and distilled prior to use. All reagents used in the syntheses were of analytical grade procured from Sigma-Aldrich or Merk Chemicals and used without further modifications.
e melting points were determined on open capillaries using SMP-10 melting point apparatus. FTIR spectra were recorded using PerkinElmer Spectrum 100 Series ATR or FT-IR instrument on KBr pellets in the range 4000-400 cm −1 . Proton and carbon-13 nuclear magnetic resonance spectra were obtained from the Bruker 400 MHz spectrometer. e chemical shifts were measured in ppm relative to a TMS standard. UV-Vis spectra were recorded in DMSO solvent at a range of 200-800 nm. Bioassays on the anticancer efficacy were performed at the Department of Biotechnology at the University of the Western Cape. e elemental microanalysis was performed on Server 112 series Elemental Analyzer at the University of Stellenbosch. e single crystal X-ray crystallography was performed at Rutgers University, USA, using a Bruker SMART CCD Apex-II area-detector. e complexes (C1-C4) were tested against human cell lines: Caco-2 (human colon), HeLa (human cervical), HepG2 (human hepatocellular), MCF-7 (breast cancer), PC-3 (human prostate), and MCF-12A (noncancer human breast) cells.
e cells were cultured in their respective media supplemented with 10% fetal bovine serum (FBS) and 1% pen-strep cocktail (100 U/mL penicillin and 100 g/ mL streptomycin). Caco-2, HeLa, HepG2, and MCF-7 cells were grown in Dulbecco's Modified Eagle Medium and MCF-12A in DMEM-F12 containing insulin, EGF, and hydrocortisone, while PC-3 cells were cultured in RPMI-1640 media. e cells were grown at 37°C in a 5% CO 2 humidified incubator (Labotec, South Africa) and seeded at 1 × 10 5 cells/mL density in a 96-well plate for 24 h. e cells were treated with 100 µg/mL of the test compound for 24 h period. Cytotoxicity of the compounds was assessed by MTT assay following manufacturer's instructions. After treatment, 10 μL of 5 mg/mL MTT (Sigma, USA) was added to each well, and the plates were incubated at 37°C for 3 h. e insoluble formazan crystals were solubilised by adding 100 μL of DMSO. e reduction of MTT was read at 570 nm using POLARStar Omega plate reader.

Synthesis of the Ligands
e ligand was synthesized using the method described by Channar et al. [9] with some modifications. iophene-2carbaldehyde (475 µl (5 mmol)) and thiosemicarbazide (0.4558 g (5 mmol)) were refluxed under inert conditions in 20 ml dry methanol for 12 hours. On cooling, a light brown precipitate was formed which was redissolved in diethyl ether, filtered on activated carbon, and kept in the fridge for slow evaporation where shiny brown crystals were obtained.

Crystal Structure for L1.
e single crystal X-ray crystallography experiment was performed using a Bruker SMART CCD Apex-II area-detector. e crystal structure was solved and refined using the full-matrix least-square Journal of Chemistry 3 method based on F 2 [10] and the graphics interface program ORTEP-3 for Windows [11].
Attempts to complex L2 with K 2 PtCl 4 and L3 with either Pd(cod)Cl 2 or K 2 PtCl 4 did not give a product. Similar attempts to complex L1 with PtCl 2 [(PPh 3 ) 2 ] 2 did not yield a product.

Infrared Spectra.
e FTIR for the compounds were recorded in either KBr pellets or ATR. e IR spectrum for the ligands displayed a clear stretching vibration bands between 1605 and 1611 cm −1 which were assigned to the imine C � N moiety. e ligand L1 has an unsubstituted thiophene and shows the highest energy for the imine bond at 1611 cm −1 . On introducing a bromide at position 4 on the thiophene ring (L3), there is a hypsochromic shift of 6 cm −1 to 1605 cm −1 . is is because of the electron withdrawing effect of the electronegative bromide which draws electron density away from the thiophene ring and consequently from the imine region thereby raising the single bond character of the imine bond resulting in the observed lower shift in the frequency. e ligand L2 with a -Br introduced at position 5 on the thiophene ring showed a lesser shift in frequency (3 cm −1 ) from 1611 cm −1 to 1608 cm −1 . Compared to L3, the -Br at position 5 has a possible resonance donation from its lone pair of nonbonding electrons which contribute to an increased electron density to the thiophene ring and consequently to the imine region. However, the electronegativity dipole is dominant compared to the resonance dipole due to the poor overlap of 4p-2p orbitals with carbon. e FTIR spectra for the ligands are shown in Table 1.
e azomethine peaks were observed in the complexes where they were found to have shifted to between 1593 and 1637 cm −1 . It was observed that, in all the Pd complexes, the azomethine peak shifted to higher energy, while for Pt(II) complexes, it shifted to lower energy in the IR spectra. For the ligands, a possible explanation to this can be deduced from a consideration of the different groups and substituents attached to the imine bond. Complexes C1 and C3 were compared to the parent ligand L1 after the introduction of PdCl 2 and PtCl 2 salts, respectively. As mentioned earlier, complexation with Pd(II) caused a shift to higher energy by 8 cm −1 (1611 cm −1 to 1619 cm −1 for C1) while complexation with Pt(II) shifted the energy to a lower wavenumber by 18 cm −1 (1593 cm −1 to 1611 cm −1 for C3).
is can be explained in terms of nuclear charge for the two metals. Pt(II) has a higher nuclear charge inferring that the incoming ligand will be attracted more to Pt than to Pd. is leaves the azomethine region with less electron density and more single bond character for the Pt(II) complex compared to the Pd(II) complex. Bond dissociation energies for M-L bond is also greater for Pt than Pd due to less steric crowding around the Pt metal center. ese factors raise the overall reactivity of Pd(II) complexes compared to Pt(II), a reason why Pd-Cl bond dissociates 10 4 -10 5 times faster in Pd(II) complexes [12].
Complex C4 was a modification of C3, where one -Cl was substituted for -PPh 3 and a -Br introduced at position 4 on the thiophene ring. e -PPh 3 group is a much better s donor and π acceptor which effectively weakens the Pt-N bond trans to itself in C4 through ground state trans-influence.
is in turn means that electron density is not drawn from the imine region, and therefore, the imine bond in C4 retains more π character compared to that in C3. However, the -Br in position 4 has minimal influence since there is no resonance donation for the nonbonding electrons. ese factors resulted in the observed difference in energy for the imine bonds, 1608 cm −1 versus 1593 cm −1 for C4 and C3, respectively.
Complex C2 was a modification of C1, where a -Br was introduced at position 5 on the thiophene ring. At position 5, there is a possible resonance donation from the halide lone pair implying that the imine bond retains more π character in C4 compared to C1, reflected in the hypsochromic shift observed in C2 (1621 cm −1 from 1608 cm −1 (L2)). e FTIR spectra data for the complexes are shown in Table 1.

1 H-NMR Spectra.
e azomethine protons together with the protons attached to the thiophene ring were observed and compared for the three ligands after introduction of the bromide substituent, as shown in Figure 1.
For L1, H a , H b , and H c occurred at 7.13, 7.45, and 7.65 ppm, respectively, while the azomethine proton occurred at 8.25 ppm. Upon introduction of a Br at position 4 (L3), the remaining protons H a and H c appeared further downfield (7.53 and 7.75 ppm, respectively), as a result of deshielding by the Br substituent. Similar trend is observed when the Br is introduced at position 5 (L2). e peaks for H a and H b now appear at 7.27 and 8.14 ppm, respectively. Together with the electronegativity of the -Br, the protons at orthoposition to -Br experience steric deshielding as the hydrogen s-orbitals are disrupted from the normal spherical symmetry. e azomethine proton for L1 appeared at 8.25 ppm. On introduction of a Br at position 4 (L3) and position 5 (L2) of the thiophene ring, an upfield shift of 0.10 ppm (to 8.16 ppm, L3) and 0.11 ppm (to 8.14 ppm, L2) was observed. is trend is expected because, at position 5, there is resonance   Journal of Chemistry donation of Br lone pair electrons; thus, the azomethine proton for L2 experiences a higher shielding effect and resonates further upfield compared to L3. e 1 H-NMR spectra data are shown in Table 1. A representative 1 H-NMR spectrum for ligand L3 is shown in Figure 2.
Upon complexation, the resonance frequencies of the azomethine protons were observed and compared to those of the free ligands. Complexes C1 and C3 were compared to the parent ligand L1, where a downfield shift was observed in both complexes. e Pd(II) complex (C1) showed a lesser shift of 0.16 ppm compared to 0.30 ppm observed in the Pt(II) complex C3. As discussed above, this can be attributed to the higher nuclear charge of Pt(II) compared to Pd(II), which causes a higher deshielding of the azomethine region in the Pt(II) complex leading to a more downfield shift for the azomethine proton. A representative 1 H-NMR spectrum for complex C1 is shown in Figure 3.
Complexes C3 and C4 differed in that there was a Br substituent attached to the thiophene ring, and the PPh 3 group coordinated to the metal center in C4, while no substituent was present in C3, and coordination to the metal was by Cl ligands. Considering C4 with a Br at position 4 and a PPh 3 directly coordinated to the metal center, the Br at position 4 has minimal resonance influence to the complex, but PPh 3 is both a good s donor and a π acceptor. e s donation is through a hybrid orbital containing a lone pair located on phosphorus, which is enhanced by the electronrich phenyl rings attached to the phosphorus. e steric bulk of the PPh 3 group and the resultant crowding around the metal center is a determinant in the rate at which the group dissociates from a metal, where the bulkier the R group, the faster the rate of dissociation [13]. ese factors together with the higher trans-influence of PPh 3 compared to Cl make C4 to be more shielded at the azomethine region compared to C3. is resulted in the observed difference of 0.59 ppm between the azomethine protons of the two complexes.
Complexes C2 and C1 differed only on the Br substituent at position 5 of the thiophene ring of C2. At position 5, the Br substituent has possible resonance donation to the adjacent π system. is increases the shielding of the azomethine proton making it to resonate at a higher field region compared to that of C1. e 1 H-NMR spectra for the complexes are shown in Table 1.

13 C-NMR Spectra.
e 13 C-NMR spectra for the ligands were compared with those of their corresponding complexes for carbons at the imine regions. e ligand imine carbons shifts occurred at 139.24 ppm, 141.07 ppm, and 140.80 ppm for L1, L2, and L3, respectively. Introduction of a -Br at position 5 (L2) had an incremental effect on the chemical shift (by 1.83 ppm) on the imine carbon compared to the -Br at position 4 (L3) which caused a shift of 1.56 ppm. At position 5, the -Br has a higher inductive effect on the ligand via the π system, which deshields the imine carbon more causing it to resonate at a higher frequency (low field). e 13 C-NMR spectra for the ligands are shown in Table 1. A representative 13 C-NMR spectrum for ligand L3 is shown in Figure 4.
After complexation, the shifts for the imine carbon of complexes C1 and C3 occurred further downfield (146.04 ppm and 145.86 ppm, respectively) compared to the parent ligand L1.
is increase in shift by 6.95 ppm and 5.28 ppm is as a result of coordination to the metal as electron density is pulled away from the azomethine bond deshielding the carbon nucleus.
is means that only a smaller external magnetic field is necessary to bring the nucleus into resonance, resulting in the observed higher chemical shifts in 13 C-NMR. Similar trend is observed for complexes C4 and C2 compared to the parent ligands. A representative 13 C-NMR spectrum for complex C2 is shown in Figure 5.

Electronic Spectra.
UV-visible spectra for the compounds were recorded in DMSO at range 200-800 nm using quartz cells at a concentration of 1.0 × 10 −3 M. e results for the photophysical data are summarized in Table 1.
As shown in Table 1, a higher bathochromic shift (7 nm) was observed in L2 after introducing Br at position 5 of the thiophene ring than in L3 (3 nm) with the -Br at position 4. An auxochrome at position 5, as opposed to position 4, has better p-π conjugation with the rest of the π system from the possible resonance donation of the lone pair on -Br. is increased conjugation led to the observed hyperchromic effect in L2.
e complexes had different metal centers and ligands coordinated to the metal. C1 and C3 differed only by the type of metal center. e absorbance for C3 with a Pt (II) metal center occurred at a shorter wavelength (348 nm) compared to C1 (364 nm) with a Pd(II) metal center. A possible reason for this is the higher nuclear charge of Pt(II) which draws electron density away from the π system effectively lowering the energy of π orbitals thereby increasing the ΔE between π-π * levels in C3. C1 and C2 differed only by the presence of a -Br in position 5 of C2. e presence of the auxochrome increased the electron density of the π bonding orbitals resulting in raised energy level through electronelectron repulsion, leading to the observed longer wavelength in C2.
C4 and C3 differed in that there was a -Br substituent in position 4 of the thiophene ring, and a bulky -PPh 3 coordinated to the metal center of C4. PPh 3 is a better s donor-π acceptor compared to Cl, and the electron-rich phenyl rings impart it with better ligand to metal charge transfer properties causing the observed red shift in C4.
e UV-Vis spectra for the complexes are displayed in Table 1.
In general, ligand spectra showed peaks corresponding to π ⟶π * transitions with molar extinction coefficients of 10 3 LMol −1 cm −1 , while the complexes exhibited an extra broad and weak absorptions at around 550-570 nm assigned to d-d transitions, with molar extinction coefficients of 10 1 -10 2 LMol −1 cm −1 . In contrast, the spectra for all the complexes displayed two peaks for C1 and C2 and three peaks for C3 and C4. Similar observations are reported in literature and are attributed to a combination of the ligand based π-π * and MLCT [(dπ (metal) −π * (ligand) ] [14]. e UV-Vis spectra for complex C3 is shown in Figure 6.

Crystal Structure for Ligand L1.
Crystals suitable for X-ray crystallography were grown for ligand L1 by slow diffusion of hexane into a THF solution of L1. e ligand belongs to the monoclinic P21/n space system with 8-unit molecules packed into the crystal unit. e structure data and refinement parameters are shown in Table 2. e structure showed the thiosemicarbazone existing in the thione form. e molecular pair adopts a different conformation for each unit molecule with one molecule lying on a perfect plane but the other having a torsion angle of about 17° (  Figure 7(a)). e molecule is stabilized through intermolecular hydrogen bonding between the hydrogen attached to N-5 of one molecule and thiosemicarbazide sulphur of the other molecules. Furthermore, hydrogen bonding extends towards the adjacent molecular pair, as shown in Figure 7(b).

Journal of Chemistry
Proton scans over a 72 h period were conducted to establish stability in solution, as shown in Figure 8. Lack of any changes in peaks over the test period indicated that the compounds were stable in solution and therefore could be studied for bioassay. e complexes were then subjected for bioassays to assess their anticancer activities.

Bioassays on Cytotoxicity.
e main objective of this work was to evaluate thiosemicarbazone-based Pd(II) and Pt(II) complexes for possible anticancer properties. e motivation behind this study was two-fold. First, the sterically bulky substituents around the metal center are a strategy appearing in literature for prevention of axial approach to the metal atom from the z 2 -direction. is hinders     the formation of a trigonal bipyramid (TBP) intermediate which would lead to a ligand substitution [15] and thereby lead to high binding selectivity to DNA in vitro and in vivo [16] Secondly, it has been shown that bidentate chelation plays a significant role in preventing trans-labilization and unwanted dislodgment of ligands in vivo [17,18]. Preliminary results with the free ligands did not show any substantial activity either as anticancer agents, and therefore, the detected activity could be accredited to the complexed forms. e anticancer activity was calculated according to the following equation: % cell viability � average absorbances of treated cells average absorbances of control e results obtained against a control under similar test conditions with no test compound added are shown in Figure 9.
Structure-activity correlations were drawn on the different trends in cytotoxicity of these complexes. Complex C1 was similar to C2 differing only by a -Br substituent on position 5 of the thiophene moiety of C2. Comparing the results for these two complexes, the introduction of the -Br (C2) resulted in remarkable difference in activity, where cell viability in all cell lines Caco-2 (8%), HepG2 (5%), HeLa (38%), MCF-7 (6%), MCF-12A (5%), and PC-3 (49%) increased remarkably. e difference in the results for C1 and C2 could be attributed to the presence of -Br in C2 which decreased the electron density around the metal center. is caused the -Cl ligands to be held more firmly, which in turn decreased the rate of -Cl substitution reducing the cytotoxicity of C2. Similar observations are reported in literature where it is observed that an increase in donor properties of the coordinated groups directly leads to increased cytotoxicity for Pd drugs [19].
Complexes C1 and C3 had similar structures differing only by the metal center, Pd(II) for C1 and Pt(II) for C3. Complex C1 was found to be more cytotoxic than C3 in all the tested cells. Since Pd(II) has a lower nuclear charge compared to Pt(II), the ligands are less strongly held in C1.
e smaller spatial size of 4d-orbitals in Pd (II) compared to 5d-orbitals in Pt (II) also led to more steric crowding in the Pd (II) centre which probably resulted in higher rates of ligand substitution, raising the cytotoxicity in C1. e observed higher cytotoxicity in C4 in comparison to C3 could be attributed to the steric crowding effects of the bulky PPh 3 group in C4 since the steric bulk of a PR 3 group and the resultant crowding around the metal center is a determinant in the rate at which the group dissociates from the metal. Tolman [13] working on nickel complexes made similar observations where steric hindrance played a bigger role than electronic effects in influencing the rate of attaining equilibrium in a number of phosphorus ligands on nickel(0) [13]. e expected higher ligand dissociation determined the observed higher cytotoxicity for C4 compared to C3 with a Cl group. e plain ligands did not show any substantial activity at the tested dose (data not shown) compared to their corresponding complexes, and therefore, the reduced cell proliferation shown could be accredited to the complex compounds.  Table 3.

DNA-Binding Studies.
Spectroscopy is widely used in the study of binding modes for metal complexes by observing the alterations that appear in the λ max absorption values of π-π * intraligand transitions, ligand⟶metal charge transfers, or on the d-d transitions, as the DNA concentration is serially increased to a solution of a metal complex. Binding modes are then inferred from the spectra, whereby an intercalative mode results in a hypochromic shift and bathochromic shift or hypsochromism. Intercalation is as a result of overlap of π * antibonding orbitals of the ligands bound to the complex with π bonding orbitals of the DNA base pairs. is decreases the probable transitions, and the effect is observed as   12 Journal of Chemistry hypochromic response [20]. On the contrary, a hyperchromic shift suggests electrostatic mode of binding. e spectral shift in the metal complex absorption is correlated to the binding strength from which the kinetics can then be determined [21].
Observations on the changes occurring in the UV-Vis spectra of a compound during serial additions of DNA is an accepted procedure in studying the binding modes and kinetics of DNA-complex interactions [22]. In this study, we used calf thymus-DNA (CT-DNA) prepared in 10 mM Tris-HCl buffer at pH 7.29. e DNA concentration was calculated from the λ max of 260 nm using the molar absorptivity of the CT-DNA and ε � 6600 M −1 . e ratio of the absorbance (A 260 /A 280 ) was found to be 1.918 which assured that DNA was free of protein [23].
Serial concentrations of calf thymus DNA (CT-DNA) were titrated to a fixed concentration of the complexes in the cuvette and scanned from 200-800 nm. e mixture was allowed to incubate for 5 minutes prior to taking UV-Vis measurements. With continued addition of DNA, the peaks of interest eventually decreased up to a point where they disappeared, and at the same time, there appeared a peak at 260 nm. is clearly showed that all the complex had been bound to DNA and further additions resulted in excess free DNA in the mixture which was indicated by the appearance of a characteristic DNA peak at 260 nm. e binding kinetics for the complex-DNA interaction was then determined by the intrinsic binding constant, K b , by plots of the Benesi-Hildebrand equation [24] and shown as follows: where From the binding constant values, Gibbs free energy changes, ΔG, for the complex DNA interactions were calculated using the following equation: where R is the gas constant and T is the absolute temperature. e absorption spectra of the interaction of CT-DNA with the complexes together with the Benesi-Hildebrand plots are shown in Figures 10-13.
All the complexes exhibited hypochromic shifts at λ max . e hypochromism is probably the result of intercalative mode of binding as a result of the overlap of π * antibonding orbitals of the ligands bound to the complex, with π bonding orbitals of the DNA base pairs [25].
is decreases the probable transitions, and the effect is observed as a hypochromic shift [20].
Furthermore, distinct isosbestic points appeared at 283 nm in the spectra of C2 and C4 and 292 nm for C3.
is is as a result of equilibrium between bound and free 0 0   form of DNA and indicates that there are no other species in the mixture [26]. Binding constant and Gibbs free energy values were then evaluated and compared to those of common DNA intercalators, as shown in Table 4. Complex C1 showed higher values compared to those of the known DNA intercalators lumazine, epirubicin, and proflavine, indicating a strong binding between these complexes and DNA. Complex C3 showed a lower binding constant probably due to the presence of the Br substituent. Since intercalation generally arises from the overlap of π * -orbitals of intercalator with the π-orbitals DNA base pairs [30], the presence of an electronegative substituent conjugated to the π-system of an intercalator will remove electron density, thereby reducing the reactivity of the system. is may have contributed to the low binding profile of C2.
As shown in Table 4, all the ΔG values were negative, an indication of the spontaneity of interaction during the complex-DNA formation process [28].

Conclusion
is work produced new complexes of Pd(II) and Pt(II) with insights into tuning the physical-chemical properties and the resultant biological effects. Synthesis, isolation, and purification were all performed under mild laboratory conditions. e suggested structures were confirmed by elemental microanalysis and X-ray crystallography for one of the ligands.  Binding profiles with DNA were studied using CT-DNA and UV-Vis spectroscopy, where they exhibited hypochromic shifts at λ max which indicated an intercalative binding mode. Furthermore, the intrinsic DNA-binding constants, k b , (M −1 ) of 3.7031 × 10 4 (C1), 1.7298 × 10 4 (C3), and 1.8962 × 10 4 (C4) and Gibbs free energy (ΔG kJ mol −1 ) values ranging from 24.04 to 26.03 are compared to some of the available well-known intercalators further suggesting this mode of binding. Anticancer tests against selected cancer cells in vitro showed that their activities correlated with their corresponding structures, where the different ligands around the metal center effected different rates of ligand substitution, which reflected on the observed cytotoxicity profiles. is was most notable on C2, which was a modification of C1 after introduction of -Br to position 5 of thiophene ring. is caused a remarkable increase in cell viability from 11% to 48% in HeLa cells and 28% to 78% in PC-3 cells and a difference of 37% and 50%, respectively.

Data Availability
e data used to support these findings, i.e., FTIR peaks, 1 H-NMR peaks, 13 C-NMR peaks, and UV-Vis peaks, for all the compounds together with the calibration curve used to determine the CT-DNA concentration are included within the supplementary information file which has been attached as a separate PDF document. e figures are arranged as follows: (1)  e crystallographic structure for ligand L1 has been deposited with Cambridge Crystallographic Data Centre, CCDC 1885726. A Copy of this data may be found from CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK (fax: +44-1223-336033 or by e-mailing deposit@ccdc.cam.ac.uk or going to the website http://www.ccdc.cam.ac.uk).

Conflicts of Interest
e authors declare that they have no conflicts of interest.