BIS(4-FLUOROPHENYLSULFONYLDITHIOCARBIMATO)ZINCATE(II) SALTS: NEW ANTIFUNGALS FOR THE CONTROL OF Botrytis BLIGHT

Abstract

Botrytis blight or gray mold is a highly destructive disease caused by Botrytis spp., that infects flowers, trees vegetables, fruit, especially grapevines and strawberry. Three new compounds with general formula (A)₂[Zn(4-FC₆H₄SO₂N=CS₂)₂], where A = PPh₃CH₃ (2a), PPh₃C₂H₅ (2b), PPh₃C₄H₉ (2c), and the previously published compounds where A = PPh₄ (2d) and NBu₄ (2e), were synthesized by the reaction of 4-fluorophenylsulfonyldithiocarbimate potassium dihydrate and zinc(II) acetate dihydrate with the appropriate counter cations (A) halides. The new compounds were characterized by infrared, ¹H and ¹³C NMR spectroscopies. All these salts inhibited the growth of Botrytis cinerea, with compounds 2c and 2d showing greater antifungal activity than zinc dimethyldithiocarbamate, the active principle of the fungicide Ziram. The bis(dithiocarbimate)zincate(II) salts are also active against the bacteria Escherichia coli and Staphylococcus aureus.

Keywords
dithiocarbimates; antimicrobial activity; Botrytis cinerea ; Escherichia coli ; Staphylococcus aureus

INTRODUCTION

Several bis(dithiocarbamato)-zinc(II) complexes have been used as agrochemicals mainly due to their high efficiency in controlling plant fungal diseases, and relatively low toxicity.^1,2 However, there is a continuing need for replacement of active ingredients and formulations to meet the environmental requirements, as well as avoiding resistance mechanisms.³ In these perspectives and due to the structural similarity with dithiocarbamates, we have been investigating the antifungal activity of salts containing anionic bis(N-R-sulfonyldithiocarbimato)zincate(II) complexes.^4-6 For example, it was observed that the compound tetrabutylammonium bis(4-fluorophenylsulfonyldithiocarbimato)zincate(II) (2e) was very active against Colletotrichum gloeosporioides, an important fungus that causes the plant disease known as anthracnose in fruit trees.⁴

Unlike the neutral dithiocarbamate analogues, the bis(dithiocarbimate)zincate(II) complexes are anionic species that potentially offer modulation of their activity by the use of active counter ions or by varying the solubility of the salts of the complexes through the use of different cations. The activity of some phosphonium halides against various fungi and bacteria species has been reported.⁷ Thus, in this study we decided to evaluate the effect of different phosphonium cations on the antifungal activity of the anionic complex bis(4-fluorophenylsulfonyldithiocarbimate)zincate(II).

In this work, five compounds of general formula (A)₂[Zn(4-FC₆H₄SO₂N=CS₂)₂] were prepared, where A = PPh₃CH₃ (2a), PPh₃C₂H₅ (2b), PPh₃C₄H₉ (2c), PPh₄(2d) and NBu₄ (2e). The compounds 2d and 2e are described in the literature and both showed antifungal properties.^4,5 However, it was not possible to compare their effects on the fungal growth, for two different methodologies were employed.^4,5

The investigation of the influence of the different cations on the biological activity of the dithiocarbimate-zinc complexes here reported was based on the growth of Botrytis cinerea, the causal agent of the fungal disease called gray mold or Botrytis blight on fruits, vegetables and ornamental plants.⁸ For example, it is the most important post-harvest disease affecting strawberry, where the infected fruits rapidly take on a velvety, gray-brown coat of mycelium and spores. Large amounts of spores produced on each berry, when spread by air cause serious economic losses. In Brazil, there is a limited number of fungicides registered for the control of B. Cinerea. The most important classes belong to the benzimidazole and dicarboximide, for which there are reports of the occurrence of resistance of Botrytis spp.^9-13

As the activities of some phosphonium halides against bacteria have been reported, we additionally investigated the activity of the synthesized compounds against Escherichia coli and Staphylococcus aureus. Both microorganisms are very commonly associated with food-borne illnesses.^7,14 E. Coli is usually harmless, being important part of the normal gut flora. Nevertheless, some strains are poisonous to humans and other mammals. The virulent strains cause diseases such as gram-negative pneumonia, gastroenteritis, urinary tract infections and septicemia.¹⁵Although anthropic contamination of food is the main source of E. coli, it is also found in agricultural plants.¹⁶ S. aureus is also not necessarily pathogenic, being present in the skin and respiratory system of a number of healthy individuals. However, antibiotic-resistant strains are major pathogens in hospitals and long-term-care facilities.¹⁷

EXPERIMENTAL

Material and reagents

The solvents, carbon disulfide and potassium hydroxide purchased from Vetec were used without further purification. Other reagents were purchased from the trademarks: Aldrich (4-fluorobenzenesulfonamide), Vetec (zinc(II) acetate dihydrate), Alfa Aesar (tetraphenylphosphonium chloride, ethyltriphenylphosphonium chloride, 1-butyltriphenylphosphonium bromide, tetrabutylammonium bromide) and Spectrum (methyltriphenylphosphonium bromide). Uncorrected melting points were determined on a Mettler MQAPF-302 apparatus. Microanalyses for C, H and N were obtained from a Perkin-Elmer 2400 CHN elemental analyzer, and zinc was analyzed by atomic absorption with a Varian Spectra AA-200 spectrophotometer. The molar conductance (Λ_M) was measured in acetonitrile solutions at 25 ºC with a Conductivity Meter Jenway 4010. The IR spectra (4000-200 cm^-1) were recorded on a Perkin-Elmer FT-IR 1000 spectrophotometer employing the transmittance method and using CsI pellets. The ¹H (300 MHz) and ¹³C (75 MHz) NMR spectra were recorded at 20 ºC on a Varian Mercury 300 spectrophotometer in dimethyl sulfoxide-d₆ with tetramethylsilane as internal standard.

Syntheses

The 4-fluorophenylsulfonyldithiocarbimate potassium dihydrate [K₂L = K₂(4-FC₆H₄SO₂N=CS₂).2H₂O] was prepared in dimethylformamide from 4-fluorobenzenesulfonamide in reaction with carbon disulfide and potassium hydroxide, and its formation was confirmed by IR and comparison with published data.¹⁸ The bis(ditiocarbimate)-Zn(II) salts 2a-2e were prepared as shown in Figure 1.

Figure 1
Syntheses of the bis(ditiocarbimate)-Zn(II) salts

A solution of Zn(OAc)₂.2H₂O (1.0 mmol) in 1 mL of water was added to a solution of K₂L (2.0 mmol) in MeOH:H₂O 1:1 (10 mL). The reaction mixture was stirred for one hour at room temperature and then 2.0 mmol of the appropriate counter ion halide (PPh₃CH₃Br, PPh₃C₂H₅Cl, PPh₃C₄H₉Br, PPh₄Cl or NBu₄Br) previously solubilized in 2 mL of MeOH:H₂O (1:1) were added. The mixture was stirred for 30 minutes and the white solids obtained were filtered off, washed with distilled water, then drops of methanol followed by diethyl ether, and dried under reduced pressure for one day. The obtention of compounds 2d and 2e was confirmed by the comparison of their spectroscopic data and melting point values with published data.^4,5 The new compounds 2a-2c were fully characterized by NMR and infrared spectroscopy, molar conductance, melting points, elemental analyses of C, H, N and Zn, as follows.

(PPh₃CH₃)₂[Zn(4-FC₆H₄SO₂N=CS₂)₂] (2a)

Yield: 90%. M.p. 90.2 - 91.9 ºC. Anal. Calc. for C₅₂H₄₄F₂N₂O₄P₂S₆Zn: C, 55.83; H, 3.96; N, 2.50; Zn, 5.85. Found: C, 54.27; H, 4.08; N, 2.45; Zn, 5.81. IR (most important bands) (cm^-1): 3096, 3058 (υ =C-H); 2912 (υ C-H); 1374 (υ C=N); 1278 (υ_asSO₂); 1143 (υ_s SO₂); 942 (υ_as CS₂); 342 (υ ZnS). ¹H NMR (δ), J (Hz): 7.89 (s, 6H, H4'); 7.74 - 7.78 (m, 28H, H2', H3', H5', H6', H2, H6); 7.28 (t, 4H, H3, H5, ³J_H3,5-F = 8.5); 3.15 (d, 6H, H7', ²J_H7'-P= 14.6). ¹³C NMR (δ), J (Hz): 207.4 (C7); 164.1 (d, C4, ¹J_C4-F = 248.7); 139.8 (d, C1, ⁴J_C1-F = 2.7); 135.5 (d, C4', ⁴J_C4'-P = 2.7); 133.9 (d, C3', C5', ³J_C3',5'-P = 10.8); 130.8 (d, C2, C6 and C2', C6', ²J_C2',6'-P = 12.6); 120.6 (d, C1', ¹J_C1'-P = 88.3); 115.7 (d, C3, C5, ²J_C3,5-F = 22.3); 7.9 (d, C7', ¹J_C7'-P = 55.6). Λ_M(CH₃CN, S mol^-1 cm²): 238.

(PPh₃C₂H₅)₂[Zn(4-FC₆H₄SO₂N=CS₂)₂] (2b)

Yield: 92%. M.p. 74.2 - 76.0 ºC. Anal. Calc. for C₅₄H₄₈F₂N₂O₄P₂S₆Zn: C, 56.56; H, 4.22; N, 2.44; Zn, 5.70. Found: C, 54.15; H, 4.13; N, 2.46; Zn, 5.51. IR (most important bands) (cm^-1): 3098, 3062 (υ =C-H); 2942, 2908 (υ C-H); 1373 (υ C=N), 1281 (υ_asSO₂), 1143 (υ_s SO₂), 940 (υ_as CS₂), 338 (υ ZnS). ¹H NMR (δ), J (Hz): 7.89 - 7.93 (m, 6H, H4'); 7.78 - 7.84 (m, 28H, H2', H3', H5', H6', H2, H6); 7.28 (t, 4H, H3, H5, ³J_H3,5-F = 8.8); 3.53 - 3.65 (m, 4H, H7'); 1.22 (dt, 6H, H8', ³J_H8'-H7' = 7.4; ³J_H8'-P = 20.0). ¹³C NMR (δ), J (Hz): 207.4 (C7); 164.1 (d, C4, ¹J_C4-F = 248.7); 139.8 (d, C1, ⁴J_C1-F = 2.5); 135.6 (d, C4', ⁴J_C4'-P = 2.4); 134.3 (d, C3', C5', ³J_C3',5'-P = 10.0); 130.9 (d, C2', C6', ²J_C2',6'-P = 12.5); 130.8 (d, C2, C6, ³J_C2,6-F= 10.0); 118.9 (d, C1', ¹J_C1'-P = 85.6); 115.7 (d, C3, C5, ²J_C3,5-F = 22.3); 15.1 (d, C7', ¹J_C7'-P = 51.4); 6.9 (d, C8', ²J_C8'-P = 5.2). Λ_M (CH₃CN, S mol^-1 cm²): 238.

(PPh₃C₄H₉)₂[Zn(4-FC₆H₄SO₂N=CS₂)₂] (2c)

Yield: 92%. M.p. 67.5 - 69.5 ºC. Anal. Calc. for C₅₈H₅₆F₂N₂O₄P₂S₆Zn: C, 57.92; H, 4.69; N, 2.33; Zn, 5.44. Found: C, 56.49; H, 4.66; N, 2.32; Zn, 5.30. IR (most important bands) (cm^-1): 3096, 3060 (υ =C-H); 2961, 2933, 2900, 2871 (υ C-H); 1373 (υ C=N), 1280 (υ_as SO₂), 1143 (υ_sSO₂), 940 (υ_as CS₂), 338 (υ ZnS). ¹H NMR (δ), J (Hz): 7.78 - 7.90 (m, 34H, H2', H3', H4', H5', H6', H2, H6); 7.28 (t, 4H, H3, H5, ³J_H3,5-F = 7.5); 3.56 (bs, 4H, H7'); 1.49 (bs, 8H, H8', H9'); 0.89 (bs, 6H, H10'). ¹³C NMR (δ), J (Hz): 207.2 (C7); 163.9 (d, C4, ¹J_C4-F = 248.5); 139.6 (d, C1, ⁴J_C1-F = 2.6); 135.3 (d, C4', ⁴J_C4'-P = 2.4); 134.0 (d, C3', C5', ³J_{C3',5'- P} = 10.1); 130.7 (d, C2', C6', ²J_{C2',6'- P} = 12.4); 130.6 (d, C2, C6, ³J_C2,6-F = 10.0); 119.0 (d, C1', ¹J_C1'-P = 85.7); 115.5 (d, C3, C5, ²J_C3,5-F = 22.3); 24.3 (d, C9', ³J_C9'-P = 3.9); 23.6 (d, C8', ²J_C8'-P = 17.4); 20.4 (d, C7', ¹J_C7'-P = 50.0); 13.7 (s, C10'). Λ_M (CH₃CN, S mol^-1cm²): 228.

Biological assays

The antifungal activity of the zinc(II) compounds (2a-2e) was evaluated against B. cinerea by the Poisoned food technique.¹⁹ The fungus was isolated from infected strawberry tissues with gray mold symptoms. The culture medium PDA (Potato Dextrose Agar) purchased from Himedia was previously sterilized in autoclave for 20 minutes at 121 ºC. Glassware and spatulas were sterilized at 140 ºC for 3.5 h. Discs of mycelia of the fungus (diameter of 6.62 mm) were placed on the center of Petri dishes containing 15 mL of the culture medium homogeneously mixed with the substances to be tested in different concentrations, dimethyl sulfoxide (DMSO) and Tween 80 (1% v/v each). Two independent tests were carried out to check the reproducibility of the experiment, in which each sample was prepared in four repetitions and the dishes were kept in the incubator chamber at 22 ºC for three days. The control (negative check treatment) was prepared with PDA, DMSO and Tween 80 only. The positive check treatment was prepared by the same procedure using bis(dimethydithiocarbamato)zinc(II) purchased from Aldrich, Zn(DMDC)₂, the active principle of the fungicide Ziram. The diameter of the fungus colony was measured with the aid of a digital caliper every 12 hours from the second day of incubation. The effects of the parent K₂L ligand, counter cations halides (1a-1e) and Zn(OAc)₂.2H₂O were also tested under the same conditions. The percentages of inhibition were obtained after comparison with the control and the results were analyzed by polynomial regression using curves of dose employed (mM) versus percent inhibition results.

The activities of the salts (1a-1e and 2a-2e) against the bacterial strains E. coli (ATCC 11229) and S. aureus (ATCC 25923) were also studied. The liquid cultures of the microorganisms were seeded aerobically at 37 ºC in Nutrient broth and the cultures were incubated at 37 ºC for 24 h. The agar disk diffusion test was performed according to the Clinical and Laboratory Standards Institute guidelines (CLSI - Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard M02-A11, 2012). A 100 µL aliquot of overnight culture of the microorganisms corresponding to 0.5 turbidity on the McFarland scale (approximately 1.5 × 10⁸ CFU or 1.5 × 10⁸ bacteria per milliliter) was placed onto 10 mL of Nutrient agar. Suspensions of the compounds (10 µL) in DMSO at 250 mmol L^-1 were added to the paper discs (diameter of 0.5 cm). The commercial antibiotic agent norfloxacin was used as a positive control and DMSO as a negative control. The antimicrobial activities were evaluated by the presence or absence of inhibition zone around the disc and the measurements were expressed as the mean of triplicate evaluated in two independent experiments.

RESULTS AND DISCUSSION

Chemistry

Figure 2 shows the structures of compounds 2a-2e. The spectroscopic data for 2d and 2e are in accordance with the previously published data for these compounds.^4,5 The new compounds 2a-2c are white solids, stable under ambient conditions, insoluble in water, but soluble in dimethylsulfoxide, acetonitrile and chloroform. The elemental analyses of C, H, N and Zn were consistent with the proposed formulae. The molar conductance values at 10^-3 mol L^-1 in acetonitrile were in the range of 200-300 Scm² mol^-1, commonly attributed to 1:2 electrolytes.²⁰

Figure 2
Compounds 2a – 2e structures and numbering of carbon atoms of 2a – 2c for NMR attributions

The υ(CN) band in the infrared spectrum of the free ligand (K₂L) is observed at 1259 cm^-1 and a medium strong band assigned to the υ_as(CS₂) is observed at 977 cm^-1.¹⁸ The υ(CN) band was shifted to higher wavenumber values in the spectra of 2a-2c (ca. 1373 cm^-1), while the υ_as(CS₂) showed an opposite shift (to ca. 940 cm^-1). The observed shifts are consistent with the complexation of the dithiocarbimate group by two sulfur atoms.^4,5 The spectra of the complexes showed a medium-weak absorption band in the 300-350 cm^-1 range assigned to the Zn-S stretching vibration, also indicating the coordination of the gem-disulfide ligand.²¹

The integration curves on the ¹H NMR spectra of 2a-2cwere consistent with a 2:1 proportion between the cations and the bis(dithiocarbimate)zincate(II) dianions. The ¹³C NMR spectra of the salts 2a-2c showed all the expected signals for the anionic complex with approximately the same chemical shifts already published for compounds 2d and 2e.¹⁸ The C=N signal at ca. d 207 was characteristic of bis(dithiocarbimate)zincate(II) complexes, being more shielded than the C=N of the free ligand (δ 225.3).¹⁸ The aromatic carbon signals of the anionic complex were observed as doublets due to the ¹³C-¹⁹F coupling. The signal for C3 and C5 (δ ca. 115.7) was easily identified by the typical J_C-F of 22 Hz.¹⁸ The doublet for C2 and C6 (at ca. δ 130.5, J_C-F =10 Hz) was very close to the signal of the carbon atoms C2' and C6' (at ca. δ 130.8, J_C-P = 12.5 Hz) of the cations in the spectra of 2b and 2c. These signals were completely overlapped in the spectrum of 2a. The remaining signals due to the phenyl rings of the cations in the spectra of 2a-2c were similar, showing very close chemical shifts and approximately the same values of ¹³C-³¹P coupling constants. The main differences in the spectra of 2a-2c were due to the aliphatic carbon chains attached to the phosphorus atom, the chemical shifts and ¹³C-³¹P coupling constants values decreasing with the distance from the phosphorus atom, as expected.^22,23

Biological assays

The antifungal activities of the Zn(II) compounds (2a-2e) and of their parent counter cations halides (1a -1e) were evaluated against B. cinerea. The mycelial growth curves indicated that, except for the tetrabutylammonium bromide (1e), all tested compounds exhibit antifungal activity. The fungus colony growth showed a near-linear variation over time, regardless of the concentrations employed. As an example, Figure 3 presents the mycelial growth curves obtained for the compound 2d in six different concentrations. From Figure 3 it is possible to note that the inhibitory activity is already observable from the first day of incubation, with increased growth differences over the time of the experiment.

Figure 3
Colony diameter of Botrytis cinerea over 3 days of incubation at 22 °C when treated with compound 2d in different concentrations in comparison with the negative control (100% growth)

The diameters of the colony after 72 hours of incubation were used to build the curves of dose-response for each compound, as exemplified in Figure 4 for compound 2d. In all cases the second-degree polynomial model was the best fit for the experimental data, being observed correlation coefficients greater than 0.97.

Figure 4
Percent inhibition of the growth of the Botrytis cinerea colony after 3 days of incubation at 22 ºC when treated with different concentrations of 2d

The concentrations of compounds 1a-1d and 2a-2erequired to inhibit 50% in the radial growth of the colony relative to the negative control (IC₅₀) were obtained from the regression curves and the results are listed on Table 1. From the IC₅₀ values it can be observed that the nature of the R group in R-triphenylphosphonium cations influences the biological activity of the halides 1a-1d, following the decreasing order of activity: PPh₄Cl (1d) > PPh₃C₄H₉Br (1c) > PPh₃C₂H₅Cl (1b) > PPh₃CH₃Br (1a). The same trend was observed for the zinc anionic complexes salts 2a - 2d (2d > 2c > 2b > 2a). The biological activity of 1a-1d is partly related to their ability to interact with the microbial cytoplasmic membranes, one site of action of cationic biocides.⁷These results clearly indicate that the chain lengths and molecular nature of the groups affect the antifungal activity of the phosphonium salts.

Table 1
In vitro antifungal activity of the bis(dithiocarbimate)-zinc(II) salts 2a-2e, the respective countercations halides 1a-1e and bis(dimethyldithiocarbamate)zinc(II) against B. cinerea

Compounds	IC50 / mMa
1a	1.943
1b	0.878
1c	0.318
1d	0.057
1e	-
2a	0.625
2b	0.356
2c	0.109
2d	0.030
2e	1.243
Zn(DMDC)2b	0.149

• ^a
  Concentration needed to inhibit 50% of the growth of B. cinerea after 3 days of incubation at 22 ºC in comparison with the negative control;
• ^b
  Positive control: bis-dimethyldithiocarbamate-zinc(II).

Table 1 shows that 2d was the most active compound tested, being much more active than the bis(dimethyldithiocarbamato)zinc(II) (The pure active principle of Ziram) used as a positive control in the tests. It was also verified that NBu₄Br (1e) shows no inhibitory activity on mycelial growth up to 5 mM. Nevertheless, compound 2e that contains the cation NBu₄⁺ was active, presenting an IC₅₀ of 1.243 mmol L^-1. Although the IC₅₀ of 2e was higher than the values calculated for compounds 2a-2d, this value is important once it is related to the intrinsic activity of the anionic complex.

The precursor compounds K₂L and Zn(OAc)₂ were tested at the concentrations of 2.6 and 1.3 mmol L^-1, the respective molar equivalents of the ligands (L) and Zn(II) in compound 2e, and close to the observed IC₅₀ for 2e (1.243 mmol L^-1). At these concentrations, K₂L and Zn(OAc)₂ presented inhibition percentage values of 38 and 20%, respectively, while 2einhibited 50%. These results showed that the bis(dithiocarbimate)zincate(II) chelate is considerably more toxic to the fungus when compared to the parent salts.

The activity of the free ligand K₂L, the phosphonium halides 1a-1e and the complexes 2a-2e were also tested against the gram-positive and gram-negative bacteria S. aureusand E. Coli (Table 2). Tetrabutylammonium bromide (1e) was the less active compound against S. aureus and showed no activity against E. coli. Thus the activity presented by the complex 2eshows that the bis(dithiocarbimato)zincate(II) anion is at least partially responsible for the activity presented by the compounds 2a-2e(Table 2). Norfloxacin, a broad-spectrum antibiotic active against both Gram-positive and Gram-negative bacteria, was used as a positive control.

Table 2
Means of inhibition zones diameters obtained in disk diffusion assays with the bis-ditiocarbimate-zinc(II) salts 2a-2e, the respective countercations halides 1a-1e and Norfloxacin against S. aureus and E. coli

Compounds	S. aureus	E. coli
1a	20.32 ± 1.70	20.88 ± 0.96
1b	21.92 ± 1.51	22.29 ± 1.75
1c	27.10 ± 0.87	28.17 ± 1.99
1d	32.22 ± 0.06	29.95 ± 1.16
1e	11.40 ± 1.02	7.15a
2a	11.88 ± 1.56	13.68 ± 0.49
2b	13.20 ± 1.55	14.87 ± 2.02
2c	14.18 ± 0.20	12.84 ± 1.58
2d	18.82 ± 1.70	14.07 ± 0.70
2e	13.71 ± 0.48	16.31 ±1.08
Norfloxacinb	31.38 ± 0.45	29.12 ± 2.12

• ^a
  Size of the paper disc: 7.15 mm;
• ^b
  Positive control.

It was also found that the phosphonium halides 1a-1d presented larger inhibition zones than their bis(dithiocarbimato)zincate(II) salts 2a-2d. Further, most of the tested compounds exhibited shorter inhibition zones than the antibiotic norfloxacin. This observation may be a consequence of the greater difficulty of diffusion of the less hydrophilic compounds in the aqueous matrix. Thus, these tests can be regarded only as qualitative results, which showed that the tested bis-dithiocarbimate-zinc(II) phosphonium salts are active against S. aureus and E. coli.

CONCLUSIONS

Three new R-triphenylphosphonium salts of bis(4-fluorophenylsulfonyldithiocarbimato)zincate(II) (R = methyl (2a), ethyl (2b) and butyl (2c)) were synthesized. The compounds were characterized by elemental analyses, conductivity molar measurements, in addition to IR, ¹H and ¹³C NMR spectroscopies. The conductivity values and the ¹H NMR integration curves were consistent with a proportion of 2:1 for cation:anion. The shifted wavenumbers of the υ(CN) and υ_as(CS₂) vibrations compared those observed for the free ligand are in agreement with the chelation of the metal by the two sulphur atoms forming a ZnS₄ tetrahedral environment as observed for the tetraphenylphosphonium and tetrabutylammonium analogues 2d and 2e.^4,5

Except for the tetrabutylammonium bromide (1e), the phosphonium halides (1a-1d) and the bis(dithiocarbimato)zincate(II) salts 2a-2e inhibited the growth of B. cinerea. The compounds 1d, 2c and 2d showed greater antifungal activity than the dithiocarbamate Zn(DMDC)₂, the active principle of the fungicide Ziram. It was proved that the nature of the cation affects the antifungal activity of the bis-dithiocarbimate-Zn(II) salts, with increased activity in this order: NBu₄⁺ < PPh₃CH₃⁺ < PPh₃C₂H₅⁺ < PPh₃C₄H₉⁺ < PPh₄⁺. It is important to notice that the greater activity of 2d is mainly due to the cation PPh₄⁺. The counter cations halides 1a-1d and the bis(dithiocarbimate)zincate(II) salts 2a-2e were also active against E. coli and S. aureus. Thus the activity of the bis(dithiocarbimato)zincate(II) salts are worth of further investigation, especially due to their potential as antifungal agrochemicals.

• SUPPLEMENTARY MATERIAL
  IR and NMR spectra of the new compounds 2a, 2b e 2c are available at http://quimicanova.sbq.org.br, in the form of PDF file, with free access.

ACKNOWLEDGEMENTS

The authors gratefully acknowledge the Brazilian agencies CNPq, FAPEMIG and CAPES for financial support and student grants.

REFERENCES

• ¹
  Hogarth, D.; Prog. Inorg. Chem. 2005, 53, 71.
• ²
  Gullino, M. L.; Tinvella, F.; Garibaldi, A.; Kemmitte, G. M.; Bacci, L.; Sheppard, B.; Plant Dis. 2010, 94, 1076.
• ³
  Russell, P. E.; Plant Pathol. 2006, 55, 585.
• ⁴
  Alves, L. C.; Rubinger, M. M. M.; Lindemann, R. H.; Perpetuo, G. J.; Janzack, J.; Miranda, L. D. L.; Zambolim, L.; Oliveira, M. R. L.; J. Inorg. Biochem 2009, 103, 1045.
• ⁵
  Amim, R. S.; Oliveira, M. R. L.; Janczak, K.; Rubinger, M. M. M.; Vieira, L. M. M.; Alves, L. C.; Zambolim, L.; Polyhedron 2011, 30, 683.
• ⁶
  Bottega, F. C.; Oliveira, M. R. L.; Garcia, C. V.; Menezes, D. C.; Rubinger, M. M. M.; Zambolim, L.; Quim. Nova 2013, 36, 803.
• ⁷
  Kanazawa, A.; Ikeda, T.; Endo, T.; Antimicrob. Agents Chemother. 1994, 38, 945.
• ⁸
  Elad, Y.; Williamson, B.; Tudzynski, P.; Delen, N. In Botrytis: Biology, Pathology and Control; Elad, Y.; Williamson, B.; Tudzynski, P.; Delen, N., eds.; Springer: Dordrecht, 2004, pp.1-8.
• ⁹
  Yourman, L. F.; Jeffers, S. N.; Plant Dis. 1999, 83, 569.
• ¹⁰
  Leroux, P.; Chapeland, F.; Desbrosses, D.; Gredt, M.; Crop Prot. 1999, 18, 687.
• ¹¹
  Wedgea, D. E.; Smith, B. J.; Quebedeaux, J. P.; Constantin, R. J.; Crop Prot . 2007, 26, 1449.
• ¹²
  Myresiotis, C. K.; Karaoglanidis, G. S.; Tzavella-Klonari, K.; Plant Dis. 2007, 91, 407.
• ¹³
  Leroch, M.; Plesken, C.; Weber, R. W. S.; Kauff, F.; Scalliet, G.; Hahna, M.; Appl. Environ. Microbiol. 2013, 79, 159.
• ¹⁴
  Mead, P. S.; Slutsker, L.; Dietz, V.; McCaig, L. F.; Bresee, J. S.; Shapiro, C.; Griffin, P. M.; Tauxe, R. V.; Emerging Infect. Dis. 1999, 5, 607.
• ¹⁵
  Kaper, J. B.; Nataro, J. P.; Mobley, H. L. T.; Nat. Rev. Microbiol. 2004, 2, 123.
• ¹⁶
  Méric, G.; Kemsley, E. K.; Falush, D.; Saggers, E. J.; Lucchini, S.; Environ. Microbiol. 2013, 15, 487.
• ¹⁷
  Lowy, F. D.; J. Clin. Invest. 2003, 111, 1265.
• ¹⁸
  Amim, R. S.; Oliveira, M. R. L.; Perpetuo, G. J.; Janczak, J.; Miranda, L. D. L.; Rubinger, M. M. M.; Polyhedron 2008, 27, 1891.
• ¹⁹
  Singh, G.; Marimuthu, P.; Heluani, C. S.; Catalan, C. A. N.; J. Agri. Food Chem. 2006, 54, 174.
• ²⁰
  Geary, W. J.; Coord. Chem. Rev 1971, 7, 81.
• ²¹
  Nakamoto, K.; Infrared and Raman Spectra of Inorganic and Coordina tion Compounds Part B, 6^th ed., Wiley: New York, 2009.
• ²²
  Castañeda, F.; Aliaga, C.; Acuña, C.; Silva, P.; Bunton, C. A.; Phosphorus, Sulfur Silicon Relat. Elem. 2008, 183, 1188.
• ²³
  Gray, G. A.; J. Am. Chem. Soc. 1973, 95, 7736.

Data availability

https://minio.scielo.br/documentstore/1678-7064/6yqp5cGmQf9nVRqwX3DQm3y/4193e12e5a8c40cc40677686151747bfa71ace25.pdf

Publication Dates

• Publication in this collection
  July 2015

History

• Received
  18 Dec 2014
• Accepted
  26 Mar 2015