Synthesis and Antibacterial Activity of Polyoxometalates with Different Structures.

A new inorganic-organic hybrid compound, [{Cu(phen)2}2(H4W12O40)], was synthesized, and its crystal structure was determined. The Keggin anion H4W12O40 4- was grafted with two coordination units {Cu(phen)2}, forming an electrically neutral molecule. The antibacterial activity of several polyoxometalate compounds with different anionic structures including the new compound was studied. The results show that the compound 1 can inhibit the growth of Enterococcus faecalis FA2 strains and that antibacterial activity of the polyoxometalate compounds is dependent with component elements of POM but is less relative with the anion structures.

1. Instruction

<span class="Chemical">Polyoxometalatesn> (POMs) have been shown to exhibit biological ac<span class="Chemical">tivities in vitro as well as in vivo, including anticancer and antiviral [1], antibacterial [2, 3], antiprotozoal [4, 5], and antidiabetic activities [6]. In the antibacterial activity study of POMs, Tajima found the enhancement of several beta-lactams antibiotics in antibacterial activity to methicillin-resistant Staphylococcus aureus under the synergistic action of polyoxometalates, substituted-type POMs K7[PTi2W10O40] 6H2O, K7[BVW11O40]7H2O, [SiFeW11O40]6/5− and [SiCoW11O40]6− and lacunary-type POMs [XW11O39]n− (X = Si, P) and [XW9O34]n−, and proposed the resistant mechanism [7-12]. Inoue et al. reported the enhancement of antibacterial activity of beta-lactam antibiotics, oxacillin, by polyoxometalates (K6[P2W1818O62]·14H2O, K4[SiMo12O40]·3H2O, and K7[PTi2W10O40]·6H2O) against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant S. aureus (VRSA) and also proposed a reaction mechanism [13]. Daima et al. studied synergistic antibacterial action of Ag nanoparticles and POMs which were achieved by the physical damage to the bacterial cells [14]. Li and his colleagues showed the short peptides/HSiW nanofibers had antimicrobial activity to the ubiquitous and clinically relevant bacterium Escherichia coli [15]. In recent years, there are also many reports about the antibacterial activity of known and new polyoxometalate derivatives to several bacteria including Escherichia coli, Staphylococcus aureus, Paenibacillus sp., Bacillus subtilis, Clavibacter michiganensis, Vibrio sp., Pseudomonas putida, Helicobacter pylori, S. typhimurium, Streptocoque B (S. agalactiae), L. acidophilus, and amebas [3,16-34]. In these reports, the polyoxometalate derivatives are in the form of simple inorganic salts, inorganic-organic hybrids with various organic groups, films, nanofibers, etc. However, the antibacterial activity of these compounds is not satisfactory according to the reported data. Nevertheless, the emergence of multidrug-resistant bacterial strains which was partially due to the abuse of conventional antibiotics proved that there is an urgent need for novel therapeutic agents. Therefore, synthesizing and exploring new compounds with high antibacterial activity are still a challenging task of chemists and pharmacologist. To achieve this, the study on influence of the composition and structure of compounds on antibacterial activity is very important, which will play an instructional role in synthesizing and exploring new compounds.

This work is about the synthesis of a new <span class="Chemical">polyoxometalate derivative, [<span class="Chemical">Cu2(phen)4(H4W12O40)], and study on the antibacterial activity of several polyoxometalate compounds with different anionic structures including the new compound.

2. Materials and Methods

2.1. Materials and General Methods

All reagents were purchased commercially and used without further purifica<span class="Chemical">tin>on. Elemental analyses (C, H, and N) were performed on a Perkin–Elmer 2400 CHN elemental analyzer and that of W and <span class="Chemical">Cu on an ICP–AES analyzer. The IR spectrum was obtained on an Magna-560 FT/IR spectrometer with KBr pellets in the 400–4000 cm−1 region. TG analysis was carried out on a <span class="Chemical">DTG-60H thermal analyzer in flowing N2 with a heating rate of 10°C·min−1. SEM images were recorded on Hitachi S-3400N (Hitachi High-Technologies Europe GmbH, Krefeld, Germany).

2.2. Synthesis

Synthesis of [<span class="Chemical">Cu2(phen)4n>(<span class="Chemical">H4W12O40)] was modified from our previous report [35]: compound 1 was prepared from reac<span class="Chemical">tion of (NH4)6(H2W12O40)·3H2O (0.1 mmol, 0.30 g), CuCl2 2H2O (2.0 mmol, 0.34 g), phenanthroline (0.5 mmol, 0.099 g), succinic acid (0.5 mmol, 0.06 g), and 12 mL water. The starting mixture was adjusted to pH = 2.0 by the addition of hydrochloric acid, and the mixture was stirred for 1 h under air. The final solution was transferred to a 25 mL Teflon-lined autoclave and crystallized at 160°C for 96 h. Then, the autoclave was cooled at the rate of 10°C·h−1 to room temperature. The resulting green stripe crystals were filtered off, washed with distilled water, and air-dried. Good-quality crystals were sealed for structural determination and further characterization. Elemental analysis calcd for C48H32Cu2N2O41W12 (Mr = 3710) C 1.00, H 12.7619, N 2.48, O 20.68, Cu 3.38, P 1.10, W 58.60 (%); found: C 1.10, H 12.39, N 2.41, O 20.56, Cu 3.39, P 1.09, W 59.05 (%). IR(KBr pellet, cm−1): 3500, 3082, 2370, 2298, 2109, 1994, 1628, 1597, 1524, 1335, 1231, 1085, 948, 781, 750, 708, 667, 593, 530 cm−1.

Compounds 2–6 were prepared in accordance with the methods in Refs. [36-39] and characterized by the IR spectrograph and TGA.

2.3. X-Ray Crystallography

The X-ray diffrac<span class="Chemical">tin>on data of compound 1 were collected on a Bruker Smart Apex II diffractometer with <span class="Chemical">graphite monochroma<span class="Chemical">tic Mo Kα radiation (λ = 0.710 73 Å) at 293 K with ω scans (Table 1). Multiscan absorption corrections were applied. The structures were solved by direct methods and refined by full matrix least-squares on F 2 using the SHELXTL crystallographic software package [40]. The positions of hydrogen atoms on the carbon atoms were calculated theoretically. Crystal data and structure refinements for compound 1 are presented in Table 1. Cu-O and Cu-N bond lengths are listed in Table 2. CCDC-1487664 for 1 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/data_request/cif.

Table 1

Crystal data and structure refinements for compound 1.

Formula	C48H32Cu2N8O40W12
Fw	3710
Crystal system	Monoclinic
Space group	P21/c
a/Ǻ	26.1828(15)
b/Ǻ	11.84219(7)
c/Ǻ	23.3996(13)
α/˚	90.00
β/˚	113.74(2)
γ/˚	90.00
V/Ǻ3	6641.2(7)
Z	4
D c/g·cm−3	3.711
F(000)	6600
μ/mm−1	21.419
Rint	0.0932
Refine number of reflns/parameters/restraints	13661/991/54
R_factor_all/[I > 2sigma(I)]	0.0871/0.0456
wR_factor_ref/[I > 2sigma(I)]	0.0857/0.0745
Goodness of fit	0.954

Table 2

Cu-O and Cu-N bond lengths (Å) in 1.

Bond	Length	Bond	Length
Cu1 N1	2.214(11)	Cu2 N5	1.960(12)
Cu1 N2	1.990(10)	Cu2 N9	2.038(12)
Cu1 N3	1.996(13)	Cu2 N7	1.965(12)
Cu1 N4	1.991(11)	Cu2 N8	2.168(12)
Cu1 O7	2.045(10)	Cu2 O38	2.217(8)

2.4. Antibacterial Experiments

All the isolated bacterial strains were achieved by colony forma<span class="Chemical">tin>on on selec<span class="Chemical">tive salt agar plates containing 6 mg/mL <span class="Chemical">oxacillin. All bacterial strains were stored at −80°C and routinely grown at 37°C. Staphylococcus aureus (YB57), Enterococcus faecalis (FA2 and FA3), and Enterococcus faecium (SA2 and SA3) strains were cultured in brain heart infusion (BHI) broth, while Staphylococcus aureus (USA300), Acinetobacter baumannii (ABC3), and Streptococcus pneumoniae (SP) were cultured in the Luria-Bertani (LB) medium. The polyoxometalates were tested for their antibacterial activities against eight different bacterial strains by the observation of the OD value of culture media. Briefly, bacterial cells were washed and resuspended in sterile PBS, and the colony count was determined. The different polyoxometalates were added to the bacterial suspension (final concentration, 1 mg/mL), and the mixture was incubated overnight at 37°C. The colony count was determined again. Enzyme activity in vitro was expressed as the CFU reduction. As a negative control, the bacterial strains were treated with the elution buffer under the same conditions. The results are listed in Table 3.

Table 3

Antibacterial activities of compounds 1–6.

Type	Code	Compound	Concentration	Bacterial strains
I	1	[{Cu(phen)2}2(H4W12O40)]	1 mg/mL	FA2
	2	[Cu(phen)(H2O)(Mo3O10)]	1 mg/mL	ABC3, FA2, FA3, YB57, USA300
II	3	K5PW11TiO40·14H2O	1 mg/mL	YB57, USA300
III	4	Na7CeW10O35·26H2O	1 mg/mL	SA5, SA1, SP, USA300
IV	5	K13[La(SiW11O39)2]·26H2O	1 mg/mL	YB57, USA300
	6	K13[Ce(SiW11O39)2]·26H2O	1 mg/mL	SA5, SA1, SP, USA300

2.5. Scanning Electron Microscopy

Scanning electron microscopy (SEM) was performed to assess the ac<span class="Chemical">tin>vity of different <span class="Chemical">polyoxometalates on the bacterial strains in vitro. The <span class="Species">Staphylococcus aureus strains USA300 were grown to the exponential growth phase (an OD 600 nm value of 0.6) in the BHI broth at 37°C with shaking at 200 rpm. The bacteria were collected and washed three times (5,000 × g for 1 min at 4°C) with PBS. Different formulations were separately added to S. aureus suspensions. Bacterial lysates were harvested by centrifugation (1,100 × g for 1 min) at different time points. Then, the bacterial lysates were fixed with glutaraldehyde and were dehydrated and freeze-dried for SEM.

3. Results and Discussion

3.1. Crystal Structure of 1

The asymmetric unit of compound 1 consists of one <span class="Chemical">Keggin anionn> [<span class="Chemical">H4W12O40]6−, two <span class="Chemical">Cu2+ ions, and four phen molecules. The [H4W12O40]6− anion (Figure 1) contains four edge-shared W3O13 units which combine together through corner-shared linkage. W–O bonds can be classified into three sets: W–Ot (terminal oxygen atoms) with distances of 1.683(12)–1.740(12) Å, W–Ob (bridging oxygen atoms) with distances of 1.847(12)–2.010(14) Å and W–Oc (central oxygen atoms) with distances of 2.174(12)–2.396(13) Å. That is, the WO6 octahedra are all distorted. The Keggin anion acts as a bidentate ligand bonding two Cu2+ ions (Cu1 and Cu2) with one terminal oxygen atom and one bridge oxygen atom. One W-Ot bond was elongated (1.740(12) Å) due to the coordination of the terminal oxygen atom to Cu ion. Such a POM anion is also called as decorated Keggin anion (Figure 1), very similar to the decoration we reported previously [35].

Figure 1

Ball-stick representation of the decorated Keggin anion in 1.

Two <span class="Chemical">Cu2+n> ions are all five-coordinated. <span class="Chemical">Cu1 ion displays in a square prism geometry, and the geometry of <span class="Chemical">Cu2 ion is better to be described as triangle bipyramid. The donor atoms bonding to Cu ions come from two phen molecules with chelating coordination mode and the Keggin anion, forming a complex fragment {Cu(phen)2}2+ (Figure 1). Cu-O and Cu-N bond lengths are listed in Table 2. As shown in Table 2, the long bonds belong to the atoms at axial site for Cu1 and triangle plane for Cu2 (Figure S1), resulting from their environment in the crystal. Devi et al. [41] had reported a similar cluster [{Cu(phen)2}2(H2W12O40)]2·̶ in [{Cu(phen)2}4{H2W12O40}] [{Cu(phen)2}2{H2W12O40}]·3H2O, in which one Cu ion is six-coordinated, different from that of this new compound. The neutral molecules are assembled into three dimensional architecture through CH ⋯ O hydrogen bonds (Table S2) and intermolecular interaction force (Figure S2).

3.2. Characterization of 1

The IR spectrum (Figure S3) of 1 shows the vibra<n class="Species">span class="Chemical">tion absorp<spn>an class="Chemical">tion bands of CH bond in 3080 cm−1 and of C-C and N-C bonds of phen ring in 1614–1137 cm−1. The vibration absorption bands of compound 1 at 952, 877, 846, and 740 cm−1 should be ascribed to the asymmetric stretching vibrations of W-Od, W-Ob-W, and W-Oc-W bonds, respectively, consistent with that in Ref. [42]. The TG curve of 1 is shown in Figure S4. Compound 1 is stable below 400°C and then decomposes until 600°C. The lost weight of 20.17% is consistent with the calculated one (20.38% for 2H2O and 4phen), confirming the chemical formula obtained from elemental analysis and structure analysis.

3.3. Antibacterial Activity of 1–6

The compounds 1–6 used in an<span class="Chemical">tin>bacterial experiments can be divided into four kinds. 1 and 2 are inorganic-organic hybrids with <span class="Chemical">phenanthroline, and 3 is a mono-subs<span class="Chemical">tituted Keggin-type compound in which Ti atom occupies one of twelve sites. 4 is a complex of mono-lacunaria Lindquist anion and lanthanides. 5 and 6 are complexes of mono-lacunaria Keggin anions and lanthanides. From Table 3, it can be seen that (1) the new compound 1 is active only to bacterial strains FA2. (2) The compound of molybdenum, 2, has a wider antibacterial spectrum than that of tungsten (1, 3, 4, 5, 6). (3) The anionic structure has less influence on antibacterial activity. (4) The compounds with cerium element (4, 6) show better antibacterial activity than others.

SEM technique was used to explore the interac<span class="Chemical">tin>on of <span class="Chemical">polyoxometalates with the bacterial strains. SEM images (Figure 2) show the surface morphology of <span class="Species">Staphylococcus aureus strains USA300 untreated (Figure 2) and treated with 3, 4, 5, and 6 (Figures 2–2). From Figure 2, it can be seen that the surface morphology of Staphylococcus aureus strains USA300 treated with polyoxometalates (Figures 2–2) has changed obviously compared with that of untreated one (Figure 2) from smooth globular form to chapping oblate spheroid. The degree of changes in the surface morphology indicates the antibacterial activity of polyoxometalates. So, a sequence of the activity of polyoxometalates was given according to Figure 2, 4 ≈ 6 > 5 > 3. That is, the compounds with cerium element (4, 6) have better antibacterial activity than others.

Figure 2

SEM images of Staphylococcus aureus strains USA300 untreated (a) and treated with 3 (b), 4 (c), 5 (d), and 6 (e).

4. Conclusion

The bioac<span class="Chemical">tin>vity of <span class="Chemical">polyoxometalates has been known for many years but s<span class="Chemical">till has large space to explore. The results of this work on the antibacterial activity of polyoxometalates including the new compound show that antibacterial activity of the compounds is more relative with their component element than with anionic structure, which means that exploration of antibacterial materials should focus on the choice of elements.

In this work, the compounds with Ce elements have better an<span class="Chemical">tin>bacterial ac<span class="Chemical">tivity. So, synthesizing compounds with other <span class="Chemical">lanthanide elements and other compounds with cerium element and examining their antibacterial activity as well as exploring the reaction mechanism of Ce compounds need further investigations.