Sugunan, S; Suja, H; Sanjay, G; Joseph, L K; Nampoori, V P N; Radhakrishnan, P(Taylor & Francis, April 1, 2009)
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Abstract:
Thermal diffusivity (TD) measurements were performed on some industrially
important dyes – auramine O (AO), malachite green and methylene blue (MB) –
adsorbed K-10 montmorillonites using photoacoustic method. The TD value for
the dye-adsorbed clay mineral was observed to change with a variation in dye
concentration. The contribution of the dye towards TD was also determined. The
repeatedly adsorbed samples with MB and AO exhibited a lower TD than the
single-adsorbed samples. TD values of sintered MB samples were also obtained
experimentally. These sintered samples exhibit a higher TD, although they show
a trend similar to that of non-sintered pellets. A variation in dye concentration
and sintering temperature can be used for tuning the TD value of the clay mineral
to the desired level
Description:
Philosophical Magazine
Vol. 89, No. 10, 1 April 2009, 895–905
Girish Kumar,K; Joseph, Renjini(Taylor & Francis, June 1, 2009)
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Abstract:
A metalloporphyrin incorporated carbon paste sensor has been developed
for the determination of metronidazole benzoate (MTZB). Zn(II) complex
of 5,10,15,20-tetrakis (3-methoxy-4-hydroxy phenyl) porphyrin (TMHPP) was
used as the active material. The MTZB gave a well-defined reduction peak at
- 0.713V in 0.1 mol l -1 phosphate buffer solution of pH around 7. Compared
with bare carbon paste electrode (CPE), the TMHPP Zn(II) modified electrode
significantly enhanced the reduction peak current of MTZB as well as lowered
its reduction potential. Under optimum conditions the reduction peak current
was proportional to MTZB concentration over the range 1×10-3 mol1-1 to 1×10-5mol1-1. The detection limit was found to be 4.36×10-6mol1-1
. This
sensor has been successfully applied for the determination of MTZB in pharmaceutical
formulations and urine samples.
Mohammed Yusuff, K K; Robinson, P P; Arun, Vasudevan; Manju, Sebastian; Ummer Aniz, Chennampilly(Springer, June 5, 2009)
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Abstract:
The metal complex, [Ni(en)2(H2O)2](NO3)2
(en = ethylenediamine), was decomposed in a static furnace
at 200 C by autogenous decomposition to obtain
phase pure metallic nickel nanocrystallites. The nickel
metal thus obtained was studied by XRD, IR spectra, SEM
and CHN analysis. The nickel crystallites are in the
nanometer range as indicated by XRD studies. The IR
spectral studies and CHN analyses show that the surface is
covered with a nitrogen containing species. Thermogravimetric
mass gain shows that the product purity is high
(93%). The formed nickel is stable and resistant to oxidation
up to 350 C probably due to the coverage of nitrogen
containing species. Activation energy for the oxidation of
the prepared nickel nanocrystallites was determined by
non-isothermal methods and was found to depend on the
conversion ratio. The oxidation kinetics of the nickel
crystallites obeyed a Johnson–Mehl–Avrami mechanism
probably due to the special morphology and crystallite
strain present on the metal.
Prathapachandra Kurup, M R; Sheeja, S R; Sarika, Sivakumar; Neema, Ani Mangalam; Edward, R T Tiekink(Elsevier, June 23, 2009)
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Abstract:
Four hydrazone ligands: 2-benzoylpyridine benzoyl hydrazone (HBPB), di-2-pyridyl ketone nicotinoyl
hydrazone (HDKN), quinoline-2-carbaldehyde benzoyl hydrazone (HQCB), and quinoline-2-carbaldehyde
nicotinoyl hydrazone (HQCN) and four of their complexes with vanadyl salts have been synthesized and
characterized. Single crystals of HBPB and complexes [VO(BPB)(l2-O)]2 (1) and [VO(DKN)(l2-O)]2 ½H2O
(2) were isolated and characterized by X-ray crystallography. Each of the complexes exhibits a binuclear
structure where two vanadium(V) atoms are bridged by two oxygen atoms to form distorted octahedral
structures within cis-N2O4 donor sets. In most complexes, the uninegative anions function as tridentate
ligands, coordinating through the pyridyl- and azomethine-nitrogen atoms and enolic oxygen whereas in
complex [VO(HQCN)(SO4)]SO4 4H2O (4) the ligand is coordinated in the keto form. Complexes [VO(QCB)(
OMe)] 1.5H2O (3) and 4 are found to be EPR active and showed well-resolved axial anisotropy with
two sets of eight line pattern
Mohammed Yusuff, K K; Leeju, P; Arun,V; Manju, Sebastian; Varsha, Gopalakrishnan; Digna, Varghese(Crystallography Journals,Acta Crystallographica Section E ,Structure Reports, July 15, 2009)
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Abstract:
In the title molecule, C16H11N5, the mean planes of the
quinoxaline and indazole fragments form a dihedral angle of
10.62 (5). In the crystal, weak intermolecular N—H..........N
hydrogen bonds link the molecules into zigzag chains
extending in the [001] direction. The crystal packing also
exhibits pye interactions [centroid–centroid distances of
3.7080 (2) and 3.8220 (5) A ˚ ], which form stacks of the
molecules parallel to the a axis
Prathapachandra Kurup, M R; Manoj, E; Rohith, John P; Nethaji, M; Alex, Punnoose(Elsevier, July 16, 2009)
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Abstract:
An unusual copper(II) complex [Cu(L1a)2Cl2] CH3OH H2O H3O+Cl (1a) was isolated from a solution of a
novel tricopper(II) complex [Cu3(HL1)Cl2]Cl3 2H2O (1) in methanol, where L1a is 3-(2-pyridyl)triazolo
[1,5-a]-pyridine, and characterized with single crystal X-ray diffraction study. The tricopper(II) complex
of potential ligand 1,5-bis(di-2-pyridyl ketone) carbohydrazone (H2L1) was synthesized and physicochemically
characterized, while the formation of the complex 1a was followed by time-dependant monitoring
of the UV–visible spectra, which reveals degradation of ligand backbone as intensity loss of bands
corresponding to O?Cu(II) charge transfer
Girish Kumar,K; Pearl, Augustine; Sareena, John(Springer, August 29, 2009)
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Abstract:
The fabrication and electrochemical response
characteristics of two novel potentiometric sensors for the
selective determination of domperidone (DOM) are described.
The two fabricated sensors incorporate DOM–PTA
(phosphotungstic acid) ion pair as the electroactive material.
The sensors include a PVC membrane sensor and a carbon
paste sensor. The sensors showed a linear, stable, and near
Nernstian slope of 56.5 and 57.8 mV/decade for PVC
membrane and carbon paste sensors, respectively over a
relatively wide range of DOM concentration (1.0 9
10-1–1.0 9 10-5 and 1.0 9 10-1–3.55 9 10-6 M). The
response time of DOM–PTA membrane sensor was less than
25 s and that in the case of carbon paste sensor was less than
20 s.Auseful pH range of 4–6 was obtained for both types of
sensors. A detection limit of 7.36 9 10-5 M was obtained
for PVC membrane sensor and 1.0 9 10-6 M was obtained
for carbon paste sensor. The proposed sensors showed very
good selectivity toDOMin the presence of a large number of
other interfering ions. The analytical application of the
developed sensors in the determination of the drug in pharmaceutical
formulations such as tablets was investigated.
The results obtained are in good agreement with the values
obtained by the standard method. The sensors were also
applied for the determination ofDOMin real samples such as
urine by the standard addition method.
Description:
J Appl Electrochem (2010) 40:65–71
DOI 10.1007/s10800-009-9975-2
Mohammed Yusuff, K K; Manju, Sebastian; Arun, Vasudevan; Robinson, P P; Leeju, Pally; Digna, Varghese; Varsha, Gopalakrishnan(Taylor & Francis, Journal of Coordination Chemistry, October 15, 2009)
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Abstract:
The mononuclear cobalt(II) complex [CoL2] H2O (where HL is quinoxaline-2-carboxalidine-
2-amino-5-methylphenol) has been prepared and characterized by elemental analysis, conductivity
measurement, IR, UV-Vis spectroscopy, TG-DTA, and X-ray structure determination.
The crystallographic study shows that cobalt(II) is distorted octahedral with each tridentate
NNO Schiff base in a cis arrangement. The crystal exhibits a 2-D polymeric structure parallel to
[010] plane, formed by O-H...N and O-H... O intermolecular hydrogen bonds and pye
stacking interactions, as a racemic mixture of optical enantiomers. The ligand is a Schiff base
derived from quinoxaline-2-carboxaldehyde
Prathapachandra Kurup, M R; Laly, K; Suja, Krishnan(Elsevier, November 10, 2009)
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Abstract:
Five Mn(II) complexes of bis(thiosemicarbazones) which are represented as [Mn(H2Ac4Ph)Cl2]
(1), [Mn(Ac4Ph)H2O] (2), [Mn(H2Ac4Cy)Cl2]·H2O (3), [Mn(H2Ac4Et)Cl2]·3H2O (4) and
[Mn(H2Ac4Et)(OAc)2]·3H2O (5) have been synthesized and characterized by elemental analyses,
electronic, infrared and EPR spectral techniques. In all the complexes except [Mn(Ac4Ph)H2O], the
ligands act as pentadentate neutral molecules and coordinate to Mn(II) ion through two thione sulfur
atoms, two azomethine nitrogens and the pyridine nitrogen, suggesting a heptacoordination. While in
compound [Mn(Ac4Ph)H2O], the dianionic ligand is coordinated to the metal suggesting six coordination
in this case. Magnetic studies indicate the high spin state of Mn(II). Conductivity measurements reveal
their non-electrolyte nature. EPR studies indicate five g values for [Mn(Ac4Ph)H2O] showing zero field
splitting.
Mohammed Yusuff, K K; Digna, Varghese; Arun, Vasudevan; Robinson, P P; Manju, Sebastian; Leeju, P; Varsha, Gopalakrishnan(International Union of Crystallography, Acta Crystallographica Section C ,Crystal Structure Communications, November 11, 2009)
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Abstract:
The Schiff base compounds N,N0-bis[(E)-quinoxalin-2-ylmethylidene]
propane-1,3-diamine, C21H18N6, (I), and N,N0-bis[(E)-
quinoxalin-2-ylmethylidene]butane-1,4-diamine, C22H20N6,
(II), crystallize in the monoclinic crystal system. These
molecules have crystallographically imposed symmetry.
Compound (I) is located on a crystallographic twofold axis
and (II) is located on an inversion centre. The molecular
conformations of these crystal structures are stabilized by
aromatic pye stacking interactions.
The present work describes the immobilization of α-amylase over well ordered mesoporous molecular sieve SBA-15 with different pore diameters synthesized by post synthesis treatment (PST) hydrothermally after reaction at 40°C. The materials were characterized by N 2 adsorption–desorption studies, small angle X-ray diffraction, scanning electron microscopy and high resolution transmission electron microscopy. Since α-amylase obtained from Bacillus subtilis has dimensions of 35 × 40 × 70 Å it is expected that the protein have access to the pore of SBA-15 (PST-120°C) with diameter 74 Å. The pore dimension is appropriate to prevent considerable leaching. The rate of adsorption of the enzyme on silica of various pore sizes revealed the influence of morphology, pore diameter, pore volume and pH.
Prathapachandra Kurup, M R; Sreesha, Sasi; Sithambaresan, M; Fun, H K(Elsevier, 2010)
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Abstract:
Four manganese(II) complexes Mn2(paa)2(N3)4 (1), [Mn(paa)2(NCS)2] 3/2H2O (2), Mn(papea)2(NCS)2 (3),
[Mn(dpka)2(NCS)2] 1/2H2O(4) of three neutral N,N donor bidentate Schiff bases were synthesized and physico-
chemically characterized by means of partial elemental analyses, electronic, infrared and EPR spectral
studies. Compounds 3 and 4 were obtained as single crystals suitable for X-ray diffraction. Compound 4
recrystallized as Mn(dpka)2(NCS)2. Both the compounds crystallized in the monoclinic space groups P21
for 3 and C2/c for 4. Manganese(II) is found to be in a distorted octahedral geometry in both the monomeric
complexes with thiocyanate anion as a terminal ligand coordinating through the nitrogen atom. EPR spectra
in DMF solutions at 77 K show hyperfine sextets with low intensity forbidden lines lying between each
of the two main hyperfine lines and the zero field splitting parameters (D and E) were calculated.
Prathapachandra Kurup, M R; Sheeja, S R; Neema, Ani Mangalam(Elsevier, 2010)
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Abstract:
Mn(II) complexes derived from a set of acylhydrazones were synthesised and characterized by elemental
analyzes, IR, UV–vis and X-band EPR spectral studies as well as conductivity and magnetic susceptibility
measurements. In the reported complexes, the hydrazones exist either in the keto or enolate form, as evidenced
by IR spectral data. Crystal structures of two complexes are well established using single crystal
X-ray diffraction studies. In both of these complexes two equivalent monoanionic ligands are coordinated
in a meridional fashion using cis pyridyl, trans azomethine nitrogen and cis enolate oxygen atoms positioned
very nearly perpendicular to each other. EPR spectra in DMF solutions at 77 K show hyperfine sextets
and in some of the complexes the low intensity forbidden lines lying between each of the two
hyperfine lines are also observed
Sreekumar, K; Elizabeth, Chirackal Varkey(Springer, January 13, 2010)
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Abstract:
A new class of chiral polyurethanes containing
amido linkages in the polymer backbone have been synthesized
by reacting toluene diisocyanate with isosorbide
(IS) chiral moiety and the chromophores [N,N0-ethane-
1,2-diyl bis(6-hydroxy hexanamide), N,N0-butane-1,4-diyl
bis(6-hydroxy hexanamide) and N,N0-hexane-1,6-diyl bis
(6-hydroxy hexanamide)]. The corresponding chromophores
were obtained by the aminolysis of e-caprolactone by
using the diamines, diaminoethane, diaminobutane and
diaminohexane, respectively. All the polymers were synthesized
according to the symmetry conditions so as to
obtain the non-centrosymmetric environment. A series of
polyurethanes were synthesized by varying the chiral–
chromophore composition. The polyurethanes developed
were characterized by optical and thermal methods.
Description:
J Mater Sci (2010) 45:1912–1920
DOI 10.1007/s10853-009-4177-1
Prathapachandra Kurup, M R; Seena, E B; Mini, Kuriakose(Springer, February 9, 2010)
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Abstract:
Oxovanadium(IV/V) complexes of 2-hydroxyacetophenone-
3-hydroxy-2-naphthoylhydrazone (H2L)
have been synthesized and characterized. The complexes
were characterized by elemental analyses, IR, electronic
and EPR spectra. The oxovanadium(V) complex [VOL
(OCH3)] is crystallized in two polymorphic forms, denoted
by 1a and 1b, with space groups Pn21a and P 1, respectively.
Both have distorted square pyramidal structures.
Description:
Struct Chem (2010) 21:599–605
DOI 10.1007/s11224-010-9589-7
Mohammed Yusuff, K K; Varsha, Gopalakrishnan; Arun, Vasudevan; Robinson, P P; Manju, Sebastian; Digna, Varghese; Leeju, P; Jayachandran, V P(Elesvier,Tetrahedron Letters (2010), February 15, 2010)
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Abstract:
An efficient one-pot synthesis of two new heterocyclic perimidines 4-(2,3-dihydro-1H-perimidin-2-yl)-2-methoxyphenol and
2-(quinoxalin-2-yl)-2,3-dihydro-1H-perimidine in good yields is presented. This methodology provides a simple, straightforward synthetic
route to these interesting classes of heterocycles. Crystal structure, solvatochromism and antibacterial activity of these organic compounds
are discussed.
Sreekumar, K; Rajesh Krishnan, G(Taylor & Francis, February 22, 2010)
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Abstract:
Poly(amidoamine) dendrimers were synthesized on cross-linked aminomethyl polystyrene. Palladium
complexes of supported dendrimers prepared by ligand exchange method were reduced to dendrimernanoparticle
conjugates supported on polystyrene resin. The supported nanoparticles were used as
heterogeneous catalysts for the Suzuki coupling between aryl boronic acids and aryl halides. Various factors
affecting the catalysts performance were studied. Higher generation dendrimers gave well-defined
nanoparticles without agglomeration and these particles showed good catalytic performance
Prathapachandra Kurup, M R; Suma, S; Sudarsana Kumar, M R; Siji, V L(Elsevier, February 26, 2010)
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Abstract:
Eight new transition metal complexes of benzaldehyde-N(4)–phenylsemicarbazone have been synthesized
and characterized by elemental analyses, molar conductance, electronic and infrared spectral
studies. In all the complexes, the semicarbazone is coordinated as neutral bidentate ligand. 1H NMR
spectrum of [Zn(HL)2(OAc)2] shows that there is no enolisation of the ligand in the complex. The magnetic
susceptibility measurements indicate that Cr(III), Mn(II), Fe(III), Co(II) and Cu(II) complexes are
paramagnetic and Ni(II) is diamagnetic. The EPR spectrum of [Mn(HL)2(OAc)2] in DMF solution at 77K
shows hyperfine sextet with low intensity forbidden lines lying between each of the two main hyperfine
lines. The g values calculated for the [Cu(HL)2SO4] complex in frozen DMF, indicate the presence of
unpaired electron in the dx2−y2 orbital. The metal ligand bonding parameters evaluated showed strong
in-plane bonding and in-plane bonding. The ligand and complexes were screened for their possible
antimicrobial activities.
Description:
Spectrochimica Acta Part A 76 (2010) 22–28 doi:10.1016/j.saa.2010.02.035
Prathapachandra Kurup, M R; Reena, T A(Elsevier, March 15, 2010)
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Abstract:
Five copper(II) complexes [CuLCl]2·CuCl2·4H2O (1), [CuLOAc] (2), [CuLNO3]2 (3), [CuLN3] (4) and
[CuLNCS]·3/2H2O (5) of di-2-pyridyl ketone-N4-phenyl-3-semicarbazone (HL) were synthesized and
characterized by elemental analyses and electronic, infrared and EPR spectral techniques. In all these
complexes the semicarbazone undergoes deprotonation and coordinates through enolate oxygen, azomethine
and pyridyl nitrogen atoms. All the complexes are EPR active due to the presence of an unpaired
electron. EPR spectra of all the complexes in DMF at 77K suggest axial symmetry and the presence of
half field signals for the complexes 1 and 3 indicates dimeric structures
Description:
Spectrochimica Acta Part A 76 (2010) 322–327 doi:10.1016/j.saa.2010.03.011
Prathapachandra Kurup, M R; Sheena Mary, Y; Raju, K; Yohannan Panicker, C; Neema, Ani Mangalam; Hema, Tresa Varghese; Sheeja, S R(Elsevier, March 16, 2010)
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Abstract:
FT-IR spectrum of quinoline-2-carbaldehyde benzoyl hydrazone (HQb H2O) was recorded and analyzed.
The synthesis and crystal structure data are also described. The vibrational wavenumbers were examined
theoretically using the Gaussian03 package of programs using HF/6-31G(d) and B3LYP/6-31G(d) levels of
theory. The data obtained from vibrational wavenumber calculations are used to assign vibrational bands
obtained in infrared spectroscopy of the studied molecule. The first hyperpolarizability, infrared intensities
and Raman activities are reported. The calculated first hyperpolarizability is comparable with the
reported values of similar derivatives and is an attractive object for future studies of non-linear optics.
The geometrical parameters of the title compound obtained from XRD studies are in agreement with
the calculated values. The changes in the CAN bond lengths suggest an extended p-electron delocalization
over quinoline and hydrazone moieties which is responsible for the non-linearity of the molecule
Description:
Journal of Molecular Structure 973 (2010) 36–46 http://dx.doi.org/10.1016/j.molstruc.2010.03.016