Spectroscopic, thermal and biological studies on some trivalent ruthenium and rhodium NS chelating thiosemicarbazone complexes.

The synthetic, spectroscopic, and biological studies of sixteen ring-substituted 4-phenylthiosemicarbazones and 4-nitrophenyl-thiosemicarbazones of anisaldehyde, 4-chlorobenzaldehyde, 4-fluorobenzaldehyde, and vanillin with ruthenium(III) and rhodium(III) chlorides are reported here. Their structures were determined on the basis of the elemental analyses, spectroscopic data (IR, electronic, (1)H and (13)C NMR) along with magnetic susceptibility measurements, molar conductivity and thermogravimetric analyses. Electrical conductance measurement revealed a 1 : 3 electrolytic nature of the complexes. The resulting colored products are monomeric in nature. On the basis of the above studies, three ligands were suggested to be coordinated to each metal atom by thione sulphur and azomethine nitrogen to form low-spin octahedral complexes with ruthenium(III) while forming diamagnetic complexes with rhodium(III). Both ligands and their complexes have been screened for their bactericidal activities and the results indicate that they exhibit a significant activity.

1. INTRODUCTION

The synthesis and structural investigations of n class="Chemical">thiosemicarbazones and their metal complexes are of considerable centre of attention because of their potentially beneficial pharmacological properties and a wide variation in their modes of bonding and stereochemistry [1-3]. Coordination chemistry of mixed hard-soft NS donor ligands is a field of current interest. The most important factor in this objective is probably the design of ligands with an appropriate structural backbone. Thiosemicarbazones that are most widely studied are sulphur and nitrogen consisting ligands [4, 5]. Besides, thiosemicarbazones have emerged as an important sulphur containing ligands in the last two decades [6-9]. The real impetus towards coordination chemistry is the wide range of biological properties depending on parent aldehyde or ketone including antitumour [10, 11], antibacterial, and antifungal [12, 13] properties as well as their physicochemical effects [14, 15]. In addition of this, they have been screened for their medicinal properties because they possess some cytotoxic effect. They also stabilize uncommon oxidation states, generate a different coordination number in transition metal complexes in order to participate in various redox reactions [16, 17]. It is well known that several metal ions enhance and modify the biological activities of thiosemicarbazones, the new metals to such a list are ruthenium [18] and rhodium [19]. Much attention has been drawn towards the chemistry of ruthenium [20, 21] and rhodium [22] in different coordination spheres. Due to different oxidation states of ruthenium and rhodium their reactivity depends upon stability of oxidation states. In view of this ruthenium(III), thiosemicarbazones with nitrogen and sulphur as donor atoms have been found to be very efficient catalysts in the oxidation of alcohols and alkenes [23]. With the growing interest of thiosemicarbazones of ruthenium and rhodium metal ions, here we report the synthesis, characterization, and biological activities of the ruthenium(III) and rhodium(III) thiosemicarbazones obtained by condensation of the ring-substituted 4-phenylthiosemicarbazide and 4-nitrophenylthiosemicarbazide with anisaldehyde, 4-chlorobenzaldehyde, 4-fluorobenzaldehyde, and vanillin. Biological activities of the complexes and ligands have also been carried out against bacteria Bacillus subtilis and Pseudomonos aeruginosa in vitro. The ligands used in the study are of the type depicted in Figure 1.

Figure 1

Structure of the thiosemicarbazone ligands.

2. EXPERIMENTAL

2.1. Materials

RuCl and RhCl and other chemicals were purchased from Merck and Loba chemie, Bombay, India, and were used without further purification.

The antibacterial activity of the ligands and their complexes were tested by using paper disc diffusion method [24] against n class="Species">Bacillus subtilis and Pseudomonas aeruginosa. Nutrient agar medium was prepared by using peptone, beef extract, NaCl, agar-agar, distilled water, and 5 mm diameter paper discs (whatman No.1) were used. The test organisms were dissolved in ethanol to a concentrations of 1000 and 500 ppm and soaked in filter paper discs of 5 mm diameter and 1 mm in thickness. These paper discs were kept in a petri dishes (well sterilized) previously seeded with test organisms. The plates were incubated for 24–30 hours at 28 ± 2°C. The zone of inhibition was calculated in mm carefully. Streptomycin was used as standard. The composition of test media is the factor, which often exerts the greatest effect upon the drug activity. This is particularly true in the case of thiosemicarbazones.

2.2. Synthesis of the ligands

4-phenylthiosemicarbazide and n class="Chemical">4-nitrophenylthiosemicar-bazide were prepared from the appropriate amines by using a standard method [25]. The thiosemicarbazone ligands (Figure 1) were prepared by equimolar quantities of 0.02 mol of each anisaldehyde (2.72 g), 4-chlorobenzaldehyde (2.80 g), 4-fluorobenzaldehyde (2.48 g) and vanillin (3.04 g) in 10 mL ethanol with an ethanolic solution (25 mL) of 4-phenyl thiosemicarbazide (3.34 g, 0.02 mol)/4-nitrophenyl-thiosemicarbazide (4.24 g, 0.02 mol). The reaction mixtures were then refluxed on a water bath for 1 hour. Few drops of acetic acid were added during reflux. As precipitate appeared, the reaction mixture was allowed to reflux more along with stirring for 2 hours. The residue formed was separated out, filtered off, washed several times with water, recrystallized from ethanol, and finally dried in vacuo over fused calcium chloride. The proposed chemical structures of the thiosemicarbazone ligands are known to be in good agreement with the ratios concluded from analytical data (see Table 1).

Table 1

Analytical data for the ligands and their Ru(III) and Rh(III) complexes.

Compounds	M. wt. found (calcd.)	Yield (%)	Color	Analysis: found (calcd.)%						μ eff BM
				C	H	N	Cl/F	S	M
HAPT	285	70	Pale yellow	63.0	5.0	14.2	—	11.0	—	—
	(285)			(63.1)	(5.2)	(14.7)		(11.2)
HANPT	328	72	Yellow brown	54.3	3.9	16.2	—	9.5	—	—
	(330)			(54.5)	(4.2)	(16.9)		(9.6)
HCBPT	288	70	Cream yellow	57.8	3.9	14.0	12.0	11.0	—	—
	(289)			(58.1)	(4.1)	(14.5)	(12.1)	(11.0)
HCBNPT	332	75	Yellow	49.0	3.0	16.2	10.0	9.3	—	—
	(334)			(50.2)	(3.2)	(16.7)	(10.4)	(9.5)
HFBPT	271	74	Yellow	61.0	4.0	15.0	6.2	11.4	—	—
	(273)			(61.4)	(4.3)	(15.3)	(6.9)	(11.7)
HFBNPT	317	75	Yellow	52.6	3.0	17.2	5.4	10.0	—	—
	(318)			(52.8)	(3.4)	(17.6)	(5.9)	(10.0)
HVPT	300	75	Yellow brown	59.1	4.7	13.8	—	10.4	—	—
	(301)			(59.7)	(4.9)	(13.9)		(10.6)
HVNPT	345	75	Yellow	51.5	3.8	15.9	—	9.2	—	—
	(346)			(51.9)	(4.0)	(16.1)		(9.2)
[Ru(HAPT)3]Cl3	1062	68	Greenish brown	50.2	3.9	11.6	9.6	9.0	9.2	1.08
	(1063)			(50.7)	(4.2)	(11.8)	(9.8)	(9.0)	(9.5)
[Ru(HANPT)3]Cl3	1196	60	Black	44.9	3.2	13.8	8.5	8.0	8.2	1.88
	(1197)			(45.0)	(3.5)	(14.0)	(8.7)	(7.9)	(8.4)
[Ru(HCBPT)3]Cl3	1075	60	Brown	46.4	3.0	11.2	19.3	8.9	9.0	1.89
	(1076)			(46.8)	(3.3)	(11.7)	(19.5)	(8.6)	(9.3)
[Ru(HCBNPT)3]Cl3	1210	62	Black	41.3	2.5	13.2	17.1	7.9	8.0	1.78
	(1205)			(41.6)	(2.7)	(13.8)	(17.3)	(7.6)	(8.3)
[Ru(HFBPT)3]Cl3	1026	60	Dark brown	48.0	2.6	12.0	10.0	9.3	9.2	1.80
	(1027)			(49.1)	(3.5)	(12.2)	(10.2)	(9.3)	(9.8)
[Ru(HFBNPT)3]Cl3	1160	60	Black	43.1	2.6	14.2	8.8	8.2	8.4	1.90
	(1162)			(43.4)	(2.8)	(14.4)	(9.0)	(8.0)	(8.6)
[Ru(HVPT)3]Cl3	1110	60	Brown	48.2	3.7	11.1	9.2	8.6	8.9	1.68
	(1111)			(48.6)	(4.0)	(11.3)	(9.4)	(8.5)	(9.0)
[Ru(HVNPT)3]Cl3	1243	65	Black	43.0	3.1	13.2	8.2	7.7	7.9	1.70
	(1245)			(43.3)	(3.3)	(13.4)	(8.4)	(7.2)	(8.1)
[Rh(HAPT)3]Cl3	1063	70	Orange brown	50.2	3.9	11.2	9.4	9.0	9.0	—
	(1065)			(50.7)	(4.2)	(11.8)	(9.8)	(8.9)	(9.5)
[Rh(HANPT)3]Cl3	1196	65	Maroon	44.8	3.3	13.9	8.5	8.0	8.2	—
	(1198)			(45.0)	(3.5)	(14.0)	(8.7)	(8.0)	(8.5)
[Rh(HCBPT)3]Cl3	1076	60	Brown	46.5	3.0	11.2	19.2	8.9	9.3	—
	(1077)			(46.7)	(3.3)	(11.6)	(19.4)	(8.4)	(9.5)
[Rh(HCBNPT)3]Cl3	1211	65	Brown	41.2	2.4	13.3	17.1	7.9	8.2	—
	(1213)			(41.5)	(2.7)	(13.8)	(17.3)	(7.4)	(8.4)
[Rh(HFBPT)3]Cl3	1028	62	Rusty brown	48.9	3.1	11.8	10.0	9.3	9.8	—
	(1028)			(49.0)	(3.5)	(12.2)	(10.2)	(9.0)	(10.0)
[Rh(HFBNPT)3]Cl3	1162	62	Brown	43.1	2.6	14.3	8.9	8.2	8.6	—
	(1163)			(43.3)	(2.8)	(14.4)	(9.0)	(8.1)	(8.7)
[Rh(HVPT)3]Cl3	1112	60	Maroon	48.4	3.9	11.2	9.3	8.6	9.0	—
	(1113)			(48.5)	(4.0)	(11.3)	(9.4)	(8.3)	(9.1)
[Rh(HVNPT)3]Cl3	1244	68	Blackish brown	43.1	3.2	13.2	8.2	7.7	8.0	—
	(1245)			(43.3)	(3.3)	(13.4)	(8.4)	(7.2)	(8.1)

2.3. Synthesis of the complexes

[M(L)3]Cl3 (M = Ru(III), Rh(III); L = HAPT, n class="Chemical">HCBPT, HFBPT and HVPT)

Hydrated RuCl (0.261 g, 0.001 mol) and RhCl (0.263 g, 0.001 mol) in ethanol (10 mL) were heated, then n class="Chemical">metal trichloride solution was suspended in 0.003 mol of each ligand viz. HAPT (2.56 g), HCBPT (2.60 g), HFBPT (2.45 g), and HVPT (2.70 g) in ethanol (20 mL). The reaction mixtures were refluxed for 9–12 hours. The precipitates formed were cooled, filtered off, and washed with hot water, hot ethanol, and finally with diethyl ether, and dried in vacuo over fused calcium chloride. The yields were 60–70%.

[M(L)3]Cl3 (M = Ru(III), Rh(III); L = HANPT, n class="Chemical">HCBNPT, HFBNPT and HVNPT)

Hydrated RuCl (0.261 g, 0.001 mol) and RhCl (0.263 g, 0.001 mol) in ethanol (10 mL) were suspended in 20 mL ethanolic solution of the ligands viz. HANPT (2.97 g), HCBNPT (3.00 g), HFBNPT (2.86 g), and HVNPT (3.11 g). The reaction mixtures were heated for few minutes, one equivalent of ethanolic solution of the NaOH was added and the reaction mixtures were refluxed for 9-10 hours. The compound, which was precipitated out, was filtered off, washed with water, cold ethanol, and diethyl ether, and dried in vacuo over fused calcium chloride. The yields were 60–76%.

2.4. Analyses

Microanalyses were performed at Elementar Vario III Carlo Erba 1108 in Central Drug Research Institute, Lucknow, India. IR spectra of the ligands and their complexes have been recorded in KBr pellets at Shimadzu FTIR 8201 spectrophotometer in 4000–200 cm−1. Electronic spectra of the complexes were recorded in CHCl with a Perkin Elmer Lambda 15 UV/Vis spectrophotometer. 1 H and 13 C NMR were obtained with a Bruker DRX 300 spectrometer in CDCl using TMS n class="Chemical">as standard. Sulphur was estimated gravimetrically as BaSO. The percentage of nitrogen was estimated by Kjeldahl method. Magnetic susceptibility measurements on powder form of the complexes were recorded with a Gouy's balance by using mercuric tetrathiocyanato cobaltate(II) as a calibrant at 25°C. Molar conductance was carried out in 10−3 M solution of DMF. Thermogravimetric analyses were obtained at 10°C min−1 in the 25–750°C using a Shimadzu TGA-50 H analyzer. A standard method was used for determining metal ions and chlorides volumetrically and gravimetrically [26].

3. RESULTS AND DISCUSSION

The complexes were synthesized by reacting ligands with metal ion class="Chemical">ns in 3 : 1 molar ratio in ethanolic medium. Thiosemicarbazones were expected to behave as a bidentate with sulphur and nitrogen as donor atoms or coordination sites (see Figure 2). The present thiosemicarbazone ligands exist as the thione form since it has −NH−C=S thioamide group; although, in many instances, thiol form or equilibrium mixture of both forms has been observed in thiosemicarbazones. All the ruthenium(III) complexes being d5 (low spin), S = 1/2 behave as paramagnetic and rhodium(III) complexes being d6 (low spin), S = 0 act as diamagnetic. The analytical data, magnetic susceptibility, and spectral analyses agree well with the proposed composition of formed complexes. All the complexes have shown good solubility in all the common organic solvents but were found insoluble in ether, water, acetone, and benzene. All the complexes are amorphous powder, stable at room temperature and do not show any decomposition on standing for several months. The molar conductance of the complexes in DMF lies in the range 280–315 Ω−1 cm2mol−1 indicating their electrolytic behavior and confirms the ionic nature of the chloride ion. Thus the complexes may be formulated as [M(L) (where M = Ru(III), Rh(III); L = HAPT, HANPT, HCBPT, HCBNPT, HFBPT, HFBNPT, HVPT, and HVNPT).

Figure 2

Suggested structure of the complexes.

The presence of chloride ion class="Chemical">ns in outer sphere was tested both qualitatively and quantitatively and found very positive.

4. INFRARED SPECTRA

The tentative infrared absorption frequencies of the ligands and their n class="Chemical">metal complexes along with their assignments are listed in Table 2. The ligands can act either in keto or in enolic form, depending upon the conditions (e.g., pH of the medium, oxidation state of the metal ion). All physicochemical properties of the complexes support bidentate chelation of the ligands by the azomethine nitrogen and by thione sulphur. This fact was further supported by the bands including azomethine nitrogen ν(C=N) at 1610–1594 cm−1 in ligands and the lowering of this band in complexes results in chelation of the nitrogen to metal ion [27, 28]. A medium band at 1030–1020 cm−1 which is assigned to ν(N−N) in ligands is shifted to the higher frequency in the spectra of all complexes. This kind of shift on hydrazinic nitrogen described the presence of electron withdrawing substituents [29]. However, in metal complexes the band shifts to higher wave number and splits, which is probably the result of the increase in the multiplicity of the C−N bond. A strong band at 872–827 cm−1 in ligands is mainly due to the ν(C=S) stretching vibration which shifted towards lower frequency and occurred at 860–820 cm−1 in metal complexes indicating the coordination of thione sulphur to metal atom [30]. This also described a considerable change in bond order and a metal-sulphur bond. As the ν(S−H) band also remains absent, this confirms thione form of the ligand. In ligands as well as in complexes, the peak of ν(N−H) has been observed at 2842–2830 cm−1, which described no prominent change hence, deprotonation of ligands was not observed. Sharp and strong bands in continuous study of the spectra were observed as prominent peaks as ν(M−N) [31], ν(M−S) [32] at 560–520 and at 460–400 cm−1, respectively.

Table 2

Infrared spectral data (cm−1) of the ligands and its complexes. s = strong, m = medium, w = weak.

Compounds	Assignments
	ν(N−H)	ν(N−N)	ν(C=N)	ν(C=S)	ν(M−N)	ν(M−S)
HAPT	2831 s	1030 m	1594 s	827 s	—	—
HANPT	2832 s	1022 m	1600 s	860 s	—	—
HCBPT	2830 s	1020 m	1594 s	862 s	—	—
HCBNPT	2835 s	1028 m	1595 s	872 s	—	—
HFBPT	2840 s	1030 m	1610 s	830 s	—	—
HFBNPT	2835 s	1020 m	1595 s	870 s	—	—
HVPT	2842 s	1026 m	1605 s	860 s	—	—
HVNPT	2840 s	1022 m	1610 s	830 s	—	—
[Ru(HAPT)3]Cl3	2831 s	1036 m	1580 s	820 s	520 m	440 s
[Ru(HANPT)3]Cl3	2831 s	1030 m	1590 s	850 s	560 m	460 s
[Ru(HCBPT)3]Cl3	2830 s	1030 m	1585 s	852 s	535 s	400 s
[Ru(HCBNPT)3]Cl3	2834 m	1035 m	1580 s	860 s	520 m	430 s
[Ru(HFBPT)3]Cl3	2841 m	1040 m	1600 s	820 s	525 w	410 m
[Ru(HFBNPT)3]Cl3	2835 s	1025 m	1585 m	860 s	530 m	450 m
[Ru(HVPT)3]Cl3	2842 s	1032 m	1590 m	850 s	545 m	430 m
[Ru(HVNPT)3]Cl3	2841 s	1033 m	1600 s	820 s	560 m	435 s
[Rh(HAPT)3]Cl3	2830 m	1035 m	1580 s	820 s	520 m	430 w
[Rh(HANPT)3]Cl3	2832 s	1032 m	1589 m	840 s	530 w	450 w
[Rh(HCBPT)3]Cl3	2831 m	1032 m	1580 s	850 s	540 w	445 w
[Rh(HCBNPT)3]Cl3	2836 s	1035 m	1585 s	855 s	560 w	418 m
[Rh(HFBPT)3]Cl3	2841 s	1038 m	1600 s	820s	545 m	415 m
[Rh(HFBNPT)3]Cl3	2835 w	1028 m	1580 s	860 s	542 m	425 s
[Rh(HVPT)3]Cl3	2842 s	1036 m	1592 m	845 s	535 m	435 s
[Rh(HVNPT)3]Cl3	2841 s	1030 m	1598 s	820 s	532 m	440 m

5. ELECTRONIC SPECTRA

All of the formed complexes have been found to be in +3 oxidation state. Ruthenium(III) complexes act n class="Chemical">as paramagnetic one and rhodium(III) complexes are diamagnetic. Electronic spectral data are given in Table 3. The ground state of ruthenium(III) is 2T2 and the first excited doublet levels in order of increasing energy are 2A2g and 2T1g which are known to arise from t2 4e1 configuration [33]. The ruthenium(III) complexes display electronic spectra with transition at 13500–14000 cm−1, 17240–18300 cm−1, and 23280–23800 cm−1 which may be assigned to 2T2g → 4T1g, 2T2g → 4T2g, and 2T2g → 2A2g, 2T1g in increasing order of energy. The B, C, and 10 Dq parameters were calculated using the following equations [34]:

Table 3

Electronic spectral bands (cm−1) and ligand field parameters of the Ru(III) and Rh(III) complexes.

Complex	λ max (cm−1)	Assignments	ν 2/ν 1	10 Dq (cm−1)	B (cm−1)	C (cm−1)	β
[Ru(HAPT)3]Cl3	13700	2 T2g → 4 T1g (ν 1)	1.25	27342	443	2858	0.70
	17240	2 T2g → 4 T2g (ν 2)
	23600	2 T2g → 2 A2g, 2 T1g (ν 3)
[Ru(HANPT)3]Cl3	13500	-do-	1.27	27383	470	2883	0.75
	17260
	23560
[Ru(HCBPT)3]Cl3	14060	-do-	1.27	27255	475	2705	0.76
	17860
	23600
[Ru(HCBNPT)3]Cl3	13520	-do-	1.28	27352	474	2866	0.75
	17310
	23540
[Ru(HFBPT)3]Cl3	13620	-do-	1.31	27277	539	2741	0.86
	17930
	23460
[Ru(HFBNPT)3]Cl3	14000	-do-	1.30	27309	538	2656	0.86
	18300
	23580
[Ru(HVPT)3]Cl3	13510	-do-	1.33	27795	565	2865	0.90
	18030
	23800
[Ru(HVNPT)3]Cl3	14060	-do-	1.29	26875	523	2551	0.83
	18240
	23280
[Rh(HAPT)3]Cl3	17600	1 A1g → 3 T1g	1.34	21950	435	1740	0.60
	20210	1 A1g → 1 T1g (ν 1)
	27170	1 A1g → 1 T2g (ν 2)
[Rh(HANPT)3]Cl3	17550	-do-	1.35	22060	445	1780	0.62
	20280
	27400
[Rh(HCBPT)3]Cl3	17260	-do-	1.32	22615	413	1655	0.57
	20960
	27580
[Rh(HCBNPT)3]Cl3	17300	-do-	1.35	21990	442	1770	0.61
	20220
	27300
[Rh(HFBPT)3]Cl3	17400	-do-	1.37	22290	478	1910	0.66
	20380
	28020
[Rh(HFBNPT)3]Cl3	17640	-do-	1.37	22815	481	1925	0.67
	20890
	28590
[Rh(HVPT)3]Cl3	17650	-do-	1.32	22618	414	1658	0.58
	20960
	27590
[Rh(HVNPT)3]Cl3	17460	-do-	1.34	22655	444	1775	0.62
	20880
	27980

The values of these ligand field parameters are comparable to those reported for other trivalent ruthenium complexes involving n class="Chemical">nitrogen, sulphur donor molecules [35]. The values are ca. 70–90% of the free ion values. The considerable decrease in the Racah interelectronic repulsion parameter, B, suggests the presence of strong covalent bonding between the donor and the metal ions. The overall effect will be an increase in the observed Dq value; high Dq values are usually associated with considerable electron delocalization [36]. Rhodium(III) complexes exhibit electronic spectra with transitions at 17260–17650 cm−1, 20210–20960 cm−1, and 27170–28590 cm−1. These bands resemble to those of reported transitions for other hexacoordinated rhodium complexes [37]. The ground state for rhodium(III) ion is 1A1g in octahedral field, although in many instances only 1A1g → 1T1g spin allowed ligand field transitions to be observed. These transitions correspond to the 1A1g → 3T1g, 1A1g → 1T1g, and 1A1g → 1T2g, respectively, which agree well with an octahedral geometry. The B and 10 Dq values were calculated from the positions of their electronic bands using the following equations:

The ratios of the energies of ν 2 and ν 1 are in the range 1.32–1.37. The B values are 57–67% of the free ion value. The decrease in B values from the free ion value suggests that there is a con class="Chemical">nsiderable orbital overlap with strong covalency in the metal ligand σ bond [38].

6. MAGNETIC MOMENTS

The room temperature magnetic moments of all the ruthenium(III) n class="Chemical">thiosemicarbazone complexes lie in the range 1.08–1.90 B.M., which are expected to be lower than the predicted value of 2.10 B.M. This lowering may occur due to the presence of lower symmetry ligand fields, metal-metal interactions, or extensive electron delocalization in species [39]. Rhodium(III) complexes are diamagnetic and, as expected, this is again consistent with octahedral geometry of nitrogen and sulphur atoms producing a strong field [40].

6.1. 1H and 13C NMR

Coordination of thiosemicarbazones in the n class="Chemical">rhodium(III) complexes are further confirmed by 1 H and 13 C NMR spectra (see Table 4). The resonance for methoxy protons appeared as a singlet at δ 3.65 ppm in ligands and in complexes no significant change was observed. Significant azomethine proton signal, due to CH=N, was observed at δ 8.02–9.02 ppm region as a multiplet in ligands, and in complexes it has shown a change as a downfield shift and occurred at δ 8.20–9.20 ppm, indicating involvement of nitrogen in coordination. The proton peak of N−H group at δ 10.6–11.2 ppm remains the same in the ligands, and in the complexes it suggested that deprotonation do not occur and it has also shown keto form of the ligands. The multiplets as strong bands in region δ 6.2–8.2 ppm were assigned to aromatic ring protons, which also shifted downfield in the complexes.

Table 4

NMR spectral data (δ, ppm) of the thiosemicarbazones and their rhodium(III) complexes.

Compounds	1H−				13C−
	δ(CH=N)	δ(N−H)	δ(Ar−H)	δ(OCH3)	δ(C=N)	δ(C=S)	δ(O−CH3)
HAPT	8.02 (s)	10.9 (s)	6.2–7.0 (m)	3.62 (s)	162.3	179.2	65.0
HANPT	8.06 (s)	11.0 (s)	6.2–7.8 (m)	3.65 (s)	162.6	179.6	65.2
HCBPT	8.08 (s)	11.0 (s)	6.2–7.6 (m)	—	163.2	180.0	—
HCBNPT	8.06 (s)	11.2 (s)	6.2–7.8 (m)	—	163.8	180.3	—
HFBPT	9.00 (s)	10.9 (s)	6.3–7.2 (m)	—	165.0	179.8	—
HFBNPT	9.02 (s)	11.1 (s)	6.6–8.0 (m)	—	165.2	180.2	—
HVPT	9.02 (s)	11.0 (s)	6.8–8.0 (m)	3.60 (s)	164.2	179.5	65.0
HVNPT	8.08 (s)	11.2 (s)	6.2–7.8 (m)	3.61 (s)	163.9	180.2	65.2
[Rh(HAPT)3]Cl3	8.20 (s)	10.6 (s)	6.4–7.2 (m)	3.65 (s)	160.5	171.9	65.5
[Rh(HANPT)3]Cl3	8.28 (s)	10.9 (s)	6.5–7.6 (m)	3.66 (s)	160.8	172.2	65.5
[Rh(HCBPT)3]Cl3	8.26 (s)	11.1 (s)	6.6–7.9 (m)	—	162.0	172.6	—
[Rh(HCBNPT)3]Cl3	9.20 (s)	11.0 (s)	6.8–8.2 (m)	—	162.6	172.8	—
[Rh(HFBPT)3]Cl3	9.18 (s)	10.9 (s)	6.9–8.0 (m)	—	163.0	172.6	—
[Rh(HFBNPT)3]Cl3	9.20 (s)	11.0 (s)	6.6–8.0 (m)	—	163.0	172.8	—
[Rh(HVPT)3]Cl3	9.16 (s)	11.2 (s)	6.9–7.2 (m)	3.62 (s)	161.6	172.3	65.6
[Rh(HVNPT)3]Cl3	8.20 (s)	11.0 (s)	6.4–7.8 (m)	3.61 (s)	161.2	172.8	65.6

The 13 C NMR spectra revealed the presence of expected number of signals corresponding to different types of carbon atoms present in the compounds. In ligands n class="Chemical">as well as in complexes, −OCH3 group absorbs at δ 65.0–65.2 ppm and at δ 65.5–65.6 ppm slightly downfield to the methyl group carbon due to the deshielding of the directly attached electronegative oxygen atom. No change on complexation to this group occurs. The spectra of the ligands exhibit a strong band at δ 179.2–180.2 ppm and are assigned as C=S group. This band undergoes upfield shift of δ 7.2–7.4 ppm and occurs at δ 171.9–172.8 ppm. This has shown involvement of thione sulphur in coordination. The signals due to azomethine carbon occurred at δ 162.3–165.2 ppm as downfield peak, and on complexation they have shown shift to δ 160.5–163.0 ppm due to the resonance and also have given proof that nitrogen is involved in coordination.

7. THERMAL STUDIES

The TGA data reveal that there is a good agreement with the formulae n class="Chemical">as suggested from the elemental analyses. The first mass loss occurs within the temperature range 190–300°C, which corresponds to the removal of three chloride ions of the outer sphere as HCl. The number of chelate rings as well as the type of chelate rings around metal ions play an important role in the thermal stability and degradation of the complexes. Furthermore, it is known that the electronegativity and atomic radius of the central metal also affect the thermal stability. No endothermic peak has been observed, indicating absence of water molecule. Thermal investigations of [Ru(HAPT) support the removal of the organic part of the ligand as PhNHCS fragments in the temperature range 320–360°C. The third step corresponds to the removal of the three molecules of C at temperature range 400–480°C. Final decomposition leaves a mixed residue of Ru2O3−RuO2 at 680–695°C. The same decomposition pattern was observed for other complexes of ruthenium and rhodium leaving residues of RuO and Rh, respectively, in the temperature range 710–750°C like a carbonaceous matter.

8. ANTIBACTERIAL STUDIES

The results (Table 5) exhibit that complexes show moderate activity against n class="Species">Bacillus subtilis and Pseudomonos aeruginosa. The toxicity of the complexes was found better than parent ligand owing to the chelation theory of Tweedy [41]. The [Ru(HVPT), [Ru(HAPT), and [Ru(HVNPT) exhibited higher toxicity; this is due to the presence of electron donating group (OCH) in these complexes while in the same complexes of rhodium better toxicity was also observed. The variation in the toxicity of different complexes against various organisms depends either on the impermeability of the cells of the microbes or differences in ribosome in microbial cells [42]. The enhanced effect of complexes due to chelation could increase the lipophilicity of the central metal atom, which favours the permeation through the lipid layers of the cell wall. On the other hand, the mode of action of the compounds may involve the formation of hydrogen bonds through azomethine group of the complexes with the active centers of cell constituents resulting in the interference with normal cell process. Besides, antibacterial activity could not reach the affectivity of the streptomycin. On the basis of the above studies, the structures in Figure 2 may be formulated for the complexes.

Table 5

Antibacterial screening data of thiosemicarbazones and their Ru(III) and Rh(III) complexes.

Compounds	Inhibition zone (μgmL−1)
	Bacillus subtilis		Pseudomonos aeruginosa
	500	1000	500	1000
HAPT	7	9	8	9
[Ru(HAPT)3]Cl3	14	17	13	16
[Rh(HAPT)3]Cl3	10	12	9	12
HANPT	7	10	7	11
[Ru(HANPT)3]Cl3	12	16	11	16
[Rh(HANPT)3]Cl3	10	14	10	13
HCBPT	6	10	6	9
[Ru(HCBPT)3]Cl3	13	16	12	16
[Rh(HCBPT)3]Cl3	11	16	11	14
HCBNPT	7	10	7	11
[Ru(HCBNPT)3]Cl3	14	18	15	19
[Rh(HCBNPT)3]Cl3	12	14	13	15
HFBPT	7	9	6	10
[Ru(HFBPT)3]Cl3	13	16	13	17
[Rh(HFBPT)3]Cl3	10	13	10	12
HFBNPT	6	10	6	9
[Ru(HFBNPT)3]Cl3	14	17	13	16
[Rh(HFBNPT)3]Cl3	11	14	11	15
HVPT	9	12	9	11
[Ru(HVPT)3]Cl3	14	17	14	16
[Rh(HVPT)3]Cl3	11	14	11	13
HVNPT	8	10	9	11
[Ru(HVNPT)3]Cl3	15	18	14	18
[Rh(HVNPT)3]Cl3	12	15	12	14
Streptomycin	17	18	21	22