Anisic Acid Research Articles

Phenolic compounds and methylglyoxal in some New Zealand manuka and kanuka honeys

The principal phenolic compounds and methylglyoxal were analysed in New Zealand Leptospermum scoparium (manuka) and Kunzea ericoides (kanuka) honeys. These honeys shared six phenolic acids as primary components and differentiation was possible as relative proportions varied. Manuka honey contained an elevated concentration of a trimethoxybenzoic acid and methylglyoxal; and 2-methoxybenzoic acid and methylglyoxal concentrations were linearly correlated in fresh manuka honey. Kanuka honey contained an elevated concentration of methoxyphenyllactic acid. The concentration of the phenolic components increased with maturation in both honey types; and this profile development, along with a corresponding increase of methylglyoxal concentration, was linear in manuka honey. Nectar analysed from the plant species contained the same phenolic components as the honeys. These results demonstrated the phenolic profile could be used to differentiate the honey types, heat treatment of honey could be identified, and the presence of these components may contribute to the efficacy of these honeys in therapeutic uses.

Plants with phytotoxic potential: Wollemi pine ( Wollemia nobilis)

Herbicide resistance in annual ryegrass (ARG, Lolium rigidum) threatens the quality and yield of winter wheat crops in Australia, prompting research to discover novel natural plant compounds with herbicidal properties. Due to its novel nature and potentially interesting chemistry, the Australian native, Wollemi pine ( Wollemia nobilis), was tested for its ability to suppress ARG growth and its feasibility for use in weed control strategies. The leaf extract of Wollemi pine significantly inhibited the growth of ARG and wild radish ( Raphanus raphanistrum) in laboratory bioassays at concentrations above 1% extract. In soil trials, the 100% extract (100 g dried plant material/L) inhibited the dry weight of ARG by 25%. The addition of a wetting agent to the extract increased the suppression of ARG to 80% which was as phytotoxic as a 4-fold increase in the extract concentration (“400%” extract). Using bioassay-guided fractionation, the most phytotoxic fraction was identified and further analysed via GC/MS. Several compounds not previously identified in Wollemi pine leaf extracts have been identified, namely, 2-propylphenol, 3,4-dimethoxyphenol, 2-methoxybenzoic acid, vanillyl alcohol and isovanillic acid. These results suggest that Wollemi pine is an important potential source of compounds for the control of ARG and wild radish in winter crops.

Spectroscopic (FT‐IR, FT‐Raman, UV, 1H, and 13C NMR) and theoretical studies of m‐anisic acid and lithium, sodium, potassium, rubidium, and caesium m‐anisates

AbstractIn order to understand the nature of the interactions of biologically important ligands, it is necessary to carry out the physico‐chemical studies of these compounds with their biological targets (e.g., receptors in the cell or important cell components). Results of this study make it possible to predict some properties of a molecule, such as its reactivity, durability of complex compounds, and kinship to enzymes. In this paper the effect of alkali metal cations (Li, Na, K, Rb, and Cs) on the electronic structure of m‐methoxybenzoic acid (m‐anisic acid) was studied. The experimental IR (in solid state and solution), Raman, UV (in solid state and solution), 1H, and 13C NMR spectra of m‐methoxybenzoic acid, and its salts were registered, assigned, and analyzed. Some of the obtained results were compared with published data for o‐anisic acid and o‐anisates. The structures of anisic acid and Li, Na, and K m‐anisates were optimized at the B3LYP/6‐311++G** level. The IR, 1H, and 13C NMR spectra and NPA, ChelpG, and MK atomic charges were calculated. The change of metal along with the series: Li → Na → K → Rb → Cs caused: (1) the change in the electronic charge distribution in anisate anion that is seen via the occurrence of the systematic shifts of several bands in the experimental and theoretical IR and Raman spectra of anisates; (2) systematic 1H and 13C NMR chemical shifts; (3) hypsochromic shifts in UV spectra of salts as compared to ligands. Copyright © 2009 John Wiley & Sons, Ltd.

Thermal decomposition reaction kinetics of complexes of [Sm(o-MOBA)3bipy]2·H2O and [Sm(m-MOBA)3bipy]2·H2O

The complexes of [Sm(o-MOBA)3bipy]2·H2O and [Sm(m-MOBA)3bipy]2·H2O (o(m)-MOBA = o(m)-methoxybenzoic acid, bipy-2,2′-bipyridine) have been synthesized and characterized by elemental analysis, IR, UV, XRD and molar conductance, respectively. The thermal decomposition processes of the two complexes were studied by means of TG–DTG and IR techniques. The thermal decomposition kinetics of them were investigated from analysis of the TG and DTG curves by jointly using advanced double equal-double steps method and Starink method. The kinetic parameters (activation energy E and pre-exponential factor A) and thermodynamic parameters (ΔH ≠ , ΔG ≠ and ΔS ≠) of the second-step decomposition process for the two complexes were obtained, respectively.

Crystal structure of a ferredoxin reductase for the CYP199A2 system from Rhodopseudomonas palustris

Cytochrome P450-199A2 from Rhodopseudomonas palustris oxidizes para-substituted benzoic acids and may play a role in lignin and aromatic acid degradation pathways in the bacterium. CYP199A2 has an associated [2Fe-2S] ferredoxin, palustrisredoxin (Pux) but not a ferredoxin reductase. A genome search identified the palustrisredoxin reductase (PuR) gene. PuR was produced in Escherichia coli and shown to be a flavin-dependent protein that supports efficient electron transfer from NADH to Pux, thus reconstituting CYP199A2 monooxygenase activity (k(cat) = 37.9 s(-1) with 4-methoxybenzoic acid). The reduction of Pux by PuR shows K(m) = 4.2 microM and k(cat) = 262 s(-1) in 50 mM Tris, pH 7.4. K(m) is increased to 154 microM in the presence of 200 mM KCl, indicating the importance of ionic interactions in PuR/Pux binding. The crystal structure of PuR has been determined at 2.2 A resolution and found to be closely related to that of other oxygenase-coupled NADH-dependent ferredoxin reductases. Residues on the surface that had been proposed to be involved in ferredoxin reductase-ferredoxin binding are conserved in PuR. However, Lys328 in PuR lies over the FAD isoalloxazine ring and, together with His11 and Gln41, render the electrostatic potential of the surface more positive and may account for the greater involvement of electrostatic interactions in ferredoxin binding by PuR. Consistent with these observations the K328G mutation weakened Pux binding and virtually eliminated the dependence of PuR/Pux binding on salt concentration, thus confirming that the FAD si side surface in the vicinity of Lys328 is the ferredoxin binding site.

Antioxidant and Radical Scavenging Properties of Malva Sylvestris

Antioxidant capacity of the aqueous extract of Malva sylvestris was measured by its ability to scavenge the DPPH and superoxide anion radicals and to induce the formation of a phosphomolybdenum complex. Analysis of the extract, carried out by different chromatographic techniques, led to the isolation of eleven compounds: 4-hydroxybenzoic acid, 4-methoxybenzoic acid, 4-hydroxy-3-methoxybenzoic acid, 4-hydroxycinnamic acid, ferulic acid, methyl 2-hydroxydihydrocinnamate, scopoletin, N-trans-feruloyl tyramine, a sesquiterpene, (3R,7E)-3-hydroxy-5,7-megastigmadien-9-one, and (10E,15Z)-9,12,13-trihydroxyoctadeca-10,15-dienoic acid. The antioxidant activities of all these compounds are reported.

Molecular diversity of volatile compounds in rare willow (Salix spp.) honeydew honey: identification of chemical biomarkers

Salix spp. honeydew honey volatiles were analyzed for the first time by headspace solid-phase microextraction (HS-SPME) and ultrasonic solvent extraction (USE) followed by gas chromatography and mass spectrometry (GC, GC-MS). The use of HS-SPME and USE had advantageous results over the use of one single technique, as it provided different complementary chromatographic profiles for a comprehensive screening of the honeydew volatile composition. The volatiles with different functionality, molecular weight, and polarity were extracted and identified. High percentages of benzoic acid, phenylacetic acid, 2-hydroxybenzoic acid, 4-hydroxyphenylacetic acid with minor percentages of 4-methoxybenzoic acid, 4-hydroxyphenylethanol, and 4-hydroxybenzoic acid from USE extracts can be emphasized as volatile biomarkers of this honeydew that probably originated from Salix spp., as well as methyl salicylate identified only by HS-SPME. The application of heat treatment at 80 degrees C for 2 h did not change significantly the volatile composition of this honeydew.

Home-prepared anatase, rutile, and brookite TiO2 for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR study

TiO(2) catalysts of anatase, rutile and brookite phase were prepared at low temperature and tested for carrying out the photocatalytic partial oxidation of 4-methoxybenzyl alcohol to 4-methoxybenzaldehyde (p-anisaldehyde) in organic-free water suspensions. Traces of 4-methoxybenzoic acid and open-ring products were the only by-products present, CO(2) being the other main oxidation product. Rutile exhibited the highest yield to p-anisaldehyde (62% mol) at a rate of the same order of magnitude of that showed by the other samples. Commercial rutile and anatase photocatalysts were also used for the sake of comparison. The samples have been characterised by an in situ ATR-FTIR investigation carried out in conditions simulating the photoreaction ones.

Effect of substituent position and lithium, sodium and potassium on the electronic structure of o-, m- and p-methoxybenzoic acids

We have studied the effect of the substituent position in the ring, and lithium, sodium and potassium ions on the electronic structure of o-, m- and p-methoxybenzoic acids (anisic acids) by the use of FT-IR, FT-Raman, Ar matrix FT-IR and 1H NMR methods, and ab initio calculations at the B3LYP/6-311++G** level of theory. Characteristic shifts of the bands in the spectra and changes in the band intensities along the metal and ligand series were observed. On the basis of the obtained results we may answer the questions: (1) do the substituents in the benzene ring influence the electronic charge distribution in the carboxylic group of anisic acids and alkali metal anisates, (2) do the metal ions affect the electronic charge distribution in the methoxy group, (3) in what way do the alkali metals affect the electronic system of o-, m- and p-anisic acids? The substitution of lithium, sodium and potassium ions in the carboxylic group of o-, m- and p-anisic acids causes changes in the values of bond lengths and angles, and in the electronic charge distribution in the carboxylic group, methoxy group and aromatic ring. The influence of alkali metals on the electronic structure of the ligands is weaker than the effect of methoxy substituents. The effect of Li, Na and K ions on the aromatic ring of the ligands is mostly noticeable in the case of the ortho isomer. The carboxylic and methoxy groups situated in ortho positions in the ring weaken the effect of the alkali metals on the electronic charge distribution in the carboxylic anion and methoxy group.

The total synthesis of ( S)-2,4-dihydroxy-1-butyl (4-hydroxyl) benzoate

This study is the first synthesis of ( S)-2,4-dihydroxy-1-butyl (4-hydroxy) benzoate, a newly discovered natural product with anti-tumor properties from the fungus, Penicillium auratiogriseum. The key steps are a 1,3 diol protection followed by the coupling of p-anisic acid to the protected alcohol and subsequent de-protection steps.

Metal Binding by Humic Substances – Characterization by High-Resolution Lanthanoide Ion Probe Spectroscopy (HR-LIPS)

Abstract In ultra-low-temperature experiments at 4.7 K the luminescence of Eu(III) bound to different hydroxy- and methoxybenzoic acids and to humic substances (HS) was investigated. The benzoic acid derivatives were used as simple model compounds for common metal-binding structures in HS. The Eu(III) luminescence was directly excited by means of a pulsed dye laser, scanning through the 5D0 ← 7F0 transition of Eu(III) and subsequently high-resolution total luminescence spectra (TLS) were recorded. Based on the thorough analysis of the high-resolution TLS conclusions were drawn with respect to the number of different complexes formed and to the symmetry of the complexes. The crystal-field strength parameter Nν (B2q) was dependent on the electrostatic forces induced by the ligands as well as on the symmetry of the complexes. The formation of thermodynamically stable complexes was found to be slow even for small model ligands such as 2-hydroxybenzoic acid. Comparison between the model compounds and HS clearly revealed that the carboxylate group is the dominant binding site in HS. Indices for the formation of chelates, e. g. similar to 2-hydroxybenzoic acid, were not found for HS

Interindividual Pharmacokinetics Variability of the α4β1 Integrin Antagonist, 4-[1-[3-Chloro-4-[N′-(2-methylphenyl) ureido]phenylacetyl]-(4S)-fluoro-(2S)-pyrrolidine-2-yl] methoxybenzoic Acid (D01-4582), in Beagles Is Associated with Albumin Genetic Polymorphisms

The interindividual pharmacokinetic variability of the alpha(4)beta(1) integrin antagonist 4-[1-[3-chloro-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(4S)-fluoro-(2S)-pyrrolidine-2-yl]methoxybenzoic acid (D01-4582) was observed in beagles. The involvement of albumin genetic polymorphism in this variability was investigated. The albumin genotype was analyzed by sequencing the albumin gene from liver and blood samples. The plasma protein binding of D01-4582 was analyzed using an ultracentrifuge method. The results of the sequencing analysis of albumin cDNA revealed two single nucleotide polymorphisms, G1075T and A1422T, leading to amino acid changes of Ala335Ser, and Glu450Asp, respectively. These mutations show complete linkage. The prevalence of the mutant allele in a population of 47 dogs was 40%. The unbound fractions of D01-4582 in plasma decreased in the order of homozygous, heterozygous, and wild-type beagles. The equilibrium dissociation constants in the plasma from homozygous beagles were approximately sixfold greater than those for wild-type beagles. Prospective pharmacokinetic study using genotyped beagles demonstrated that the clearance was related to albumin genotype. The variability in clearance was well explained by changes in the unbound fractions. These results suggest that the interindividual variability in the canine pharmacokinetics of D01-4582 is related to an alteration in the binding affinity which is associated with albumin genetic polymorphisms.

Role of root-mediated interactions in phytotoxic interference of Ageratum conyzoides with rice ( Oryza sativa)

Ageratum conyzoides L. (billy goat weed; Asteraceae) is an annual invasive weed native of tropical America and has now naturalized worldwide, particularly in Southeast Asia. The present study investigated the nature and potential of root-mediated allelopathic interference of A. conyzoides against rice ( Oryza sativa). Root and shoot length and biomass accumulation of rice were significantly reduced (by 18–30%) when grown in the rhizosphere soil of the weed indicating the release of putative allelochemicals from the weed into the soil. The growth of rice was also progressively reduced in the soil amended with increasing amounts of root residues (5, 10 and 20 g kg −1 soil) of A. conyzoides. The addition of activated charcoal, an inert material with high affinity for organic biomolecules, partly ameliorated the negative effects of root residues amended in the soil. Further, there was no negative effect on the availability of soil nutrients in the root-amended soils. These were rather nutrient rich with greater electrical conductivity, and higher amount of organic matter, thus indicating no role in observed growth reduction. The reduction in allelopathic effects of root residue upon charcoal addition further indicated that putative phytotoxins released from the weed roots are water-soluble phenolic compounds. A significant amount of water-soluble phenolics were present in rhizosphere (∼6-times higher) and root-amended soils (∼5–10-fold higher) and their content was reduced (to ∼3.6–7.0-fold higher) when charcoal was added. The observed growth reduction in Ageratum rhizospheric or root-amended soils was concomitant with the amount of phenolic compounds. Upon HPLC analyses, these were identified as p-coumaric acid, gallic acid, ferulic acid, p-hydroxybenzoic acid and anisic acid. Under laboratory conditions, these phenolic acids reduced the root length and seedling weight of rice individually as well as in equimolar mixture, though no synergistic effect was noticed. The study concludes that root exudates and residues of A. conyzoides suppress the growth of rice by releasing phenolic allelochemicals into the soil rhizosphere and not through alteration of soil nutrients, and allelopathy plays a significant role in root-mediated negative interference of A. conyzoides.

Antidiabetic activity of 2-hydroxy 4-methoxy benzoic acid isolated from the roots of Hemidesmus indicus on streptozotocin-induced diabetic rats

2-Hydroxy 4-methoxy benzoic acid (HMBA) isolated from the roots of Hemidemus indicus (H. indicus ) was evaluated for its anti-diabetic activity on streptozoticin (STZ)-induced diabetic rats. HMBA, the active principle of H. indicus, was administered (500μg/kg body weight) orally to STZ-induced diabetic and non diabetic rats. The effect of HMBA on plasma glucose, insulin, glycosylated hemoglobin, liver glycogen and serum total cholesterol, HDL-cholesterol, LDL-cholesterol and triglycerides, alkaline phosphatase (ALP), aspartate transaminase (AST), alanine transaminase (ALT), γ-glutamyl transferase (γ-GT) and creatine kinase (CK). After administration of HMBA, the levels of glycosylated hemoglobin, total cholesterol, triglycerides, LDL-cholesterol were normalized in diabetic rats. It also reversed the elevated levels of AST, ALT, ALP, γ- GT and CK to near normal level. The levels of plasma insulin, glycosylated hemoglobin and liver glycogen were also restored after HMBA treatment. Thus the results of our study suggested that HMBA could help in controlling DM owing to their hypoglycemic and hypocholesterolemic effects.

Investigation of Antimicrobial Activities of Indole-3-Aldehyde Hydrazide/Hydrazone Derivatives

Background: Indoles and hydrazone-type compounds constitute an important class of compounds for new drug development in order to discover an effective compound against multi-drug-resistant microbial infections. Methods: A series of indole-3-aldehyde and 5-bromoindole-3-aldehyde hydrazide and hydrazones was evaluated for their in vitro antimicrobial activities using the 2-fold serial dilution technique against Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Escherichia coli, Bacillus subtilis and Candida albicans. The minimum inhibitory concentration (MIC) was determined for test compounds and for the reference standards sultamicillin, ampicillin, fluconazole and ciprofloxacin. Results: Compounds possessed a broad spectrum of activity having MIC values of 6.25–100 mg/ml against the tested microorganisms. Compounds 1a–1j, in particular, displayed better activity against MSRA and significant activity against S. aureus relative to ampicillin. Unexpectedly, indole nicotinic acid hydrazides showed no significant activity while indole anisic acid hydrazides displayed better activity. Conclusion: The results may be instructive to researchers attempting to gain more understanding of the antimicrobial activity of indole hydrazide/hydrazone-type compounds.

Synthesis of (±)- and (−)-Vibralactone and Vibralactone C

Mander reductive alkylation of methyl 2-methoxybenzoate with prenyl bromide and hydrolysis of the enol ether afforded methyl 6-oxo-1-prenyl-2-cyclohexenecarboxylate. This was converted in five steps (reduction of the ketone, saponification, iodolactonization, ozonolysis, and intramolecular aldol reaction) to a spiro lactone cyclopentenal. An efficient first synthesis of (+/-)-vibralactone was completed by retro-iodolactonization with activated Zn, formation of the beta-lactone (vibralactone C), and reduction of the aldehyde. Except for the novel use of an iodolactone to protect both the prenyl double bond and carboxylic acid, no protecting groups were used. A similar sequence starting with asymmetric reductive alkylation of the (2S)-2-methoxymethoxymethylpyrrolidine amide of 2-methoxybenzoic acid with prenyl bromide afforded (-)-vibralactone confirming the absolute stereochemical assignment that was based on computational methods.

Extent and Mechanism of Solvation and Partitioning of Isomers of Substituted Benzoic Acids: A Thermodynamic Study in the Solid State and in Solution

Temperature dependency of saturated vapour pressure and thermochemical characteristics of fusion processes for 2-, 3- and 4-methoxybenzoic acids (anisic acids) were measured and thermodynamic functions of sublimation, fusion, and evaporation calculated. A new approach to split specific and nonspecific energetic terms in the crystal lattice was developed. For methoxybenzoic acid isomers as well as for a number of analogous molecules, a parameter describing molecular packing density by the ratio of free volume of the molecules in the crystal lattice and van der Waals molecular volume is defined. Its relationship to Gibbs energy of sublimation and to the respective melting points was analysed. Temperature dependencies of solubility in buffers with pH 2.0 and 7.4, n-octanol and n-hexane were measured. The thermodynamic functions of solubility, solvation and transfer processes were deduced. Concentration dependence of partition coefficients for the outlined isomers was measured. Specific and nonspecific solvation terms were distinguished using the transfer from the 'inert' n-hexane to the other solvents. Comparison analysis of specific and nonspecific interactions in the solid state and in solution was carried out. A diagram enabling analysis of the mechanism of the partitioning process was applied. It was found that position of substituents essentially affects the mechanism of partitioning in buffer pH 2.0, however, at pH 7.4, the mechanism is independent of the position of the substituent.

Synthesis and antimicrobial activity of β-N-acylhydrazides of 4-aryl-2-hydroxy-4-oxo-2-butenoic (aroylpyruvic) acids

A series of β-N-(4-methoxybenzoyl)- and β-N-(3-nitrobenzoyl)hydrazides of 4-aryl-2-hydroxy-4-oxo-2- butenoic (aroylpyruvic) acids was obtained with 52 – 88% yields using the reaction of decyclization of 5-aryl-2,3-dihydrofuran-2,3-diones by hydrazides of 4-methoxybenzoic and 3-nitrobenzoic acid hydrazides in dioxane. The synthesized compounds were characterized and tested for antibacterial activity.

Crystal Structure of CYP199A2, a Para-Substituted Benzoic Acid Oxidizing Cytochrome P450 from Rhodopseudomonas palustris

CYP199A2, a cytochrome P450 enzyme from Rhodopseudomonas palustris, oxidatively demethylates 4-methoxybenzoic acid to 4-hydroxybenzoic acid. 4-Ethylbenzoic acid is converted to a mixture of predominantly 4-(1-hydroxyethyl)-benzoic acid and 4-vinylbenzoic acid, the latter being a rare example of C C bond dehydrogenation of an unbranched alkyl group. The crystal structure of CYP199A2 has been determined at 2.0-Å resolution. The enzyme has the common P450 fold, but the B′ helix is missing and the G helix is broken into two (G and G′) by a kink at Pro204. Helices G and G′ are bent back from the extended BC loop and the I helix to open up a clearly defined substrate access channel. Channel openings in this region of the P450 fold are rare in bacterial P450 enzymes but more common in eukaryotic P450 enzymes. The channel is hydrophobic except for the basic residue Arg246 at the entrance, which probably plays a role in the specificity of this enzyme for charged benzoates over neutral phenols and benzenes. The substrate binding pocket is hydrophobic, with Ser97 and Ser247 being the only polar residues. Computer docking of 4-ethylbenzoic acid into the active site suggests that the substrate carboxylate oxygens interact with Ser97 and Ser247, and the β-methyl group is located over the heme iron by Phe185, the side chain of which is only 6.35 Å above the iron in the native structure. This binding orientation is consistent with the observed product profile of exclusive attack at the para substituent. Putidaredoxin of the CYP101A1 system from Pseudomonas putida supports substrate oxidation by CYP199A2 at ∼6% of the activity of the physiological ferredoxin. Comparison of the heme proximal faces of CYP199A2 and CYP101A1 suggests that charge reversal surrounding the surface residue Leu369 in CYP199A2 may be a significant factor in this low cross-activity.

Spectra–structure relationship: Synthesis, characterization of copper(II) complexes with ibuprofenate, o-methoxybenzoate, p-ethoxybenzoate and single crystal X-ray structure determination of [ trans-Cu(en) 2(H 2O) 2](L) 2 where en = ethylenediammine, L = o-methoxybenzoate/ p-ethoxybenzoate

To investigate the spectra–structure relationship, three new copper(II) complex salts of composition [ trans-Cu(en) 2(H 2O) 2](L 1) 2 2H 2O (1), [ trans-Cu(en) 2(H 2O) 2](L 2) 2 (2) and [ trans-Cu(en) 2(H 2O) 2](L 3) 2 (3) (where L 1 = ibuprofenate, L 2 = o-methoxybenzoate and L 3 = p-ethoxybenzoate) were obtained when ethylenediamine was added to ‘Cu(L) 2’ (L = L 1/L 2/L 3) in methanol–water solution. The intermediate ‘Cu(L) 2’ salts were prepared by reaction of copper sulphate with sodium salt of ibuprofen, o-methoxybenzoic acid or p-ethoxybenzoic acid, respectively, in aqueous medium in 1:2 molar ratio. The newly synthesized complex salts have been characterized by elemental analyses, spectroscopic techniques (UV/visible and IR), magnetic moment determinations and conductance measurements. X-ray structure determination revealed an ionic structure consisting of one [ trans-Cu(en) 2(H 2O) 2] 2+, two [C 8H 7O 3] - ions in 2 and one [ trans-Cu(en) 2(H 2O) 2] 2+, two (C 9H 8O 3) - ions in 3. In these complex salts central metal ion copper(II) is coordinated by four nitrogen atoms, originating from two chelating ethylenediamine ligands and two oxygen atoms of two coordinated water molecules, showing distorted octahedral geometry around copper metal ion. Both of these structurally correlated octahedral [ trans-Co(en) 2(H 2O) 2] 2+ species have shown absorption at λ max ≈ 540 nm in the UV/visible spectrum.