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The phase separation behaviour and the viscoelastic properties of particles with non-adsorbing polymers: Part I - Experimental study

Goodwin, J.W.; Hughes, R.W.; Kwaambwa, H.M.; Reynolds, P.A. (Elseview Science B.V. www.elsevier.nl/locate/colsurfa, NaN, 2000)

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Abstract:

A series of well characterised cis-polyisoprene polymers have been added to dispersions of PHS coated PMMA particles in dodecane. At a molecular weight of 8000 g mol−1 and above, these systems showed phase separation at low particle volume fractions and above a critical polymer concentration. The rate of separation has been shown to be influenced by the viscosity of the polymer. At high polymer and particle volume fractions long lived metastable phases occurred. Above a critical concentration these were viscoelastic indicating an appreciable change in diffusion dynamics with two relaxation processes present. A significant Bingham yield stress was also observed. The Asakura Oosawa potential was not able to describe the observed rheological properties. At a molecular weight of 1000 g mol−1 no phase separation was observed. At high particle concentrations the yield stress was found to reduce with the addition of polymer. This was due to the polymer acting as a ‘solvent’ and penetrating the stabilising layer on the particles.

URI:

http://hdl.handle.net/10311/329

Files in this item: 1

Phase separation behaviour.pdf (2.723Mb)

Phenylpropanoid glycosides of Gnidia polycephala

Munkombwe N.M. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2003)

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Abstract:	Two phenylpropanoid glucosides, 2-O-b-d-glucosyloxy-4-methoxybenzenepropanoic acid and its methyl ester, together with syringin and adicardin were isolated from the stem of Gnidia polycephala and characterized by physical and spectroscopic data.
URI:	http://hdl.handle.net/10311/275

Files in this item: 2

Phenylpropanoid glycosides.pdf (2.288Mb)

Phenylpropanoid glycosides of Gnidia.pdf (155.6Kb)

Photochromism, anomalous multi-banded fluorescence and laser properties of some amino- and tosyl-amino derivative of oxadiazole

Nijegorodov, N.; Zvolinski, V.; Luhanga, P.V.C.; Mabbs, R.; Ahmad, J. (Elsevier Ltd. www.elsevier.com/locate/saa, NaN, 2006)

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The multi-banded fluorescence and laser properties of 11 new amino- and tosylamino derivatives of 2,5-di(phenyl)-1,3,4-oxadiazole and oxadiazole in various solvents at 293 K are reported. All the compounds investigated possess intra-molecular hydrogen quasi-bond (IHB) of 4.6-5.2 kcal mol-1 in the ground state. In the excited state they can undergo protolytic dissociation or intra-molecular photon-initiated transfer of proton and reveal anomalous fluorescence which cannot be explained within the framework of the Kasha and Kasha-Vavilov rules. Depending upon the excitation wavelength, solvent, concentration and pH of the medium, the compounds studied show a single, double, triple or even a four-banded fluorescence, which has not been reported earlier. The nature of multi-banded fluorescence is explained in terms of the possible photochromic processes in excited states. Quantum yields and decay times of the different fluorescence bands are reported. Anomalous dependence of quantum yield upon concentration of the solution is observed. Laser properties of the compounds studied are carefully tested. Laser action based on the fluorescence of the so-called bi-radical molecules is reported. Various possible arrangements of singlet and triplet levels of compounds investigated are discussed.

URI:

http://hdl.handle.net/10311/176

Files in this item: 2

license.txt (1.998Kb)

Photochromism, ... ivatives of oxadiazole.pdf (2.530Mb)

Photochromism, anomalous multi-banded fluorescence and laser properties of some amino- and tosyl-amino derivatives of oxadiazole

Nijegorodov, N; Zvolinski, V; Luhanga, P V C; Mabbs, R; Ahmad, J (Elsevier Science Ltd. www.elsevier.com/locate/saa, NaN, 2006)

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Abstract:

The multi-banded fluorescence and laser properties of 11 new amino- and tosylamino derivatives of 2,5-di(phenyl)-1,3,4-oxadiazole and oxadiazole in various solvents at 293K are reported. All the compounds investigated possess intra-molecular hydrogen quasi-bond (IHB) of 4.6–5.2 kcal mol−1 in the ground state. In the excited state they can undergo protolytic dissociation or intra-molecular photon-initiated transfer of proton and reveal anomalous fluorescence which cannot be explained within the framework of the Kasha and Kasha–Vavilov rules. Depending upon the excitation wavelength, solvent, concentration and pH of the medium, the compounds studied show a single, double, triple or even a four-banded fluorescence, which has not been reported earlier. The nature of multi-banded fluorescence is explained in terms of the possible photochromic processes in excited states. Quantum yields and decay times of the different fluorescence bands are reported. Anomalous dependence of quantum yield upon concentration of the solution is observed. Laser properties of the compounds studied are carefully tested. Laser action based on the fluorescence of the so-called bi-radical molecules is reported. Various possible arrangements of singlet and triplet levels of compounds investigated are discussed.

URI:

http://hdl.handle.net/10311/247

Files in this item: 2

license.txt (1.998Kb)

Nijegorodov_SAa65_2006.pdf (2.225Mb)

Prenylated arylbenzofuran derivatives from Morus mesozygia with antioxidant activity

Kapche, G.D.W.F.; Fozing, C.D.; Donfack, J.H.; Fotso, G.W.; Amadou, D.; Tchana, A.N.; Bezabih, M.; Moundipa, P F; Ngadjui, B.N.; Abegaz, B.M. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2008)

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Abstract:

Five prenylated arylbenzofurans, moracins Q–U, were isolated from Morus mesozygia (Moraceae). Their structures were elucidated on the basis of spectroscopic evidence. Along with these compounds, 3b-acetoxyurs- 12-en-11-one, marsformoxide, moracin C, moracin M, moracin K, artocarpesin, cycloartocarpesin, morachalcone A were also isolated. Four of the five compounds, (moracins R–U) displayed potent antioxidant activity.

URI:

http://hdl.handle.net/10311/315

Files in this item: 1

Prenylated arylbenzofuran.pdf (3.853Mb)

Prenylated chalcones, flavone and other constituents of the twigs of Dorstenia angusticornis and Dorstenia barteri var. subtriangularis

Ngadjui, B.; Watchueng, J.; Keumedjio, F.; Ngameni, B.; Simo, I.; Abegaz, B. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2004)

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Abstract:

The twigs of Dorstenia angusticornis and Dorstenia barteri var. subtriangularis yielded 16 compounds. Two novel diprenylated chalcones: 3,50-di-(2-hydroxy-3-methylbut-3-enyl)-4,20,40-trihydroxychalcone, 3, 4-(2,2-dimethylpyrano)-30-(2-hydroxy-3-methylbut- 3-enyl)-20,40-dihydroxychalcone and the known stipulin were isolated from both species. 3-(2-Hydroxy-3-methylbut-3-enyl)- 50-(3,3-dimethylallyl)-4,20,40-trihydroxychalcone and the known compounds: 4-hydroxylonchocarpin, kanzonol B, bartericins A, B, C and 30-(2-hydroxy -3-methylbut-3-enyl)-4,20,40-trihydroxychalcone were isolated from D. barteri while the known compounds: gancaonin Q, paratocarpins C, F, and lupeol were obtained from Dorstenia angusticornis. b-Sitosterol and its b-D-glucopyranoside were isolated from both species. Structures of these secondary metabolites were established using spectroscopic analysis, especially, NMR spectra in conjunction with 2D experiments, COSY, HMQC and HMBC.

URI:

http://hdl.handle.net/10311/253

Files in this item: 2

license.txt (1.998Kb)

Prenylated chalcones, flavone.pdf (3.563Mb)

Prenylated flavonoids and other constituents from the twigs of Dorstenia angusticornis (Moraceae)*

Simo, I.K.; Ngadjui, B.T.; Abegaz, B.M. (Elsevier Ltd. www.elsevier.com/locate/biochemsyseco, June 18, 2005)

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Abstract:

Dorstenia (Moraceae) is a mainly tropical genus of some 170 species (Mabberley, 1987). There are 23 species in Cameroon where a decoction of the leaves is administered for the treatment of cough, headache and stomach pain (Bouquet, 1969). The genus is made up largely of herbaceous perennials with succulent and non-succulent scrambling rhizomes (Berg et al., 1989). The twigs of Dorstenia angusticornis were collected in February 2002 from Kumba South West Province of Cameroon. Voucher specimen (No 28165/sfcam) is deposited at the National Herbarium Yaounde, Cameroon.

URI:

http://hdl.handle.net/10311/255

Files in this item: 1

Prenylated flavonoids and other constituents.pdf (1.986Mb)

Prenylated flavonoids, monoterpenoid furanocoumarins and other constituents from the twigs of Dorstenia elliptica (Moraceae)

Abegaz, B.M.; Ngadjui, B.T.; Folefoc, G.N.; Fotso, S.; Ambassa, P.; Bezabih, M.; Dongo, E.; Rise, F.; Petersen, D. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2003)

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Abstract:

A monoprenylated flavan and two monoterpenoid substituted furanocoumarins were isolated from the twigs of Dorstenia elliptica along with 3-(3,3-dimethylallyl)-4,20,40-trihydroxylchalcone, psoralen, bergapten, O-[3-(2,2-dimethyl-3-oxo-2H-furan-5-yl)butyl] bergaptol, b-sitosterol and its b-d-glucopyranoside. The structure of the flavan was determined as 6(1,1-dimethylallyl)-7,40- dihydroxylflavan and the monoterpenoid substituted furanocoumarins were assigned as O-[3-(2,2-dimethyl-3-oxo-2H-furan-5-yl)-3- hydroxybutyl]-bergaptol and O-[2-(5-hydroxy-2,6,6-trimethyl-3-oxo-2H-pyran-2-yl)ethyl]bergaptol, respectively, using spectroscopic analysis, especially, 2D NMR spectra.

URI:

http://hdl.handle.net/10311/286

Files in this item: 1

Prenylated flavonoids,.pdf (3.692Mb)

Progress in the chemistry of marketed traditionally used plants of Ethiopia

Abegaz, B.M. (Chemical Society of Ethiopia. http://www.aau.edu.et/faculties/sc/CSE/home.html, NaN, 1996)

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URI: http://hdl.handle.net/10311/345

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progress in the chemistry of.pdf (922.3Kb)

Quality and Compositional Studies of Some Edible Leguminosae Seed Oils in Botswana

Ketshajwang, K.K.; Holmback, J.; Yeboah, S.O. (AOCS Press. http://www.springerlink.com/content/120382/, NaN, 1998)

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Abstract:

Seed oils were extracted with n-hexane from three edible Leguminosae seeds: Tylosema esculentum, Xanthocercis zambesiaca, and Bauhinia petersiana, giving yields of 48.2, 17.6, and 20.8% (w/w), respectively. Some physical and chemical parameters were determined to ascertain the general characteristics of the oils. The saponification and iodine values indicated that all three oil samples could be classified among the olive group of oils. This inference was supported by the results of the detailed fatty acid composition of the oils as determined by capillary gas chromatography. The ratio of total unsaturated to total saturated fatty acids in all three oil samples was approximately 70:30, with either oleic or linoleic acid being the dominant fatty acid. These results were in agreement with a proton nuclear magnetic resonance analysis of the fatty acid classes in the seed oils. Thus, the analysis served to justify the use of the three Leguminosae seed oils in food preparations. The work has further indicated that, with their attractive properties, the seed oils from T. esculentum, X. zambesiaca, and B. petersiana are good candidates for further studies to evaluate their future commercial prospects in the Southern African region.

URI:

http://hdl.handle.net/10311/304

Files in this item: 1

quality and compositional.pdf (1.683Mb)

Reaction of a bulky phosphite with [Ru3(CO)12]: the molecular structure of one of the decomposition products

Magwaza, A.O.; Meijboom, R.; Muller, A.; Mavunkal, I.J. (Elsevier B.V. www.elsevier.com/locate/ica, NaN, 2008)

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Abstract:

Mono- and bis-substituted phosphite complexes [Ru3(CO)12 x Lx] (L = tris(2,4-di-tert-butylphenyl) phosphite; x = 1, 2) were synthesized by simple substitution reactions, and were characterized by spectroscopic methods. The monosubstituted ruthenium complex disproportionates in acetone producing a mononuclear ruthenium complex as one of the decomposition products. Single crystal X-ray diffraction analysis established the molecular structure of this new compound.

URI:

http://hdl.handle.net/10311/259

Files in this item: 2

license.txt (1.998Kb)

Reaction of a bulky phosphite with [Ru3(CO)12].pdf (1.989Mb)

Recent results from natural product research at the University of Botswana

Majinda, R.R.T; Abegaz, B.M.; Bezabih, M.; Ngadjui, B.T; Wanjala, C.C.W.; Mdee, L.K.; Bojase, G.; Silayo, A.; Masesane, I.; Yeboah, S.O. (IUPAC. http://www.iupac.org/publications/pac/, NaN, 2001)

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Abstract:

Marketed plants are very important items of trade in many parts of the world. The community uses these for a variety of purposes such as foods, cosmetics, flavors, spices, and medicines. It seems that plants that are used for medicinal purposes form the most common category. Four plants used for treatment of microbial infections, viz., Bolusanthus speciosus, Erythrina latissima, Crotalaria podocarpa, and Elephantorrhiza goetzei, were investigated, and these yielded several known and novel structures, some with appreciable antibiotic activity against the test organisms. The activity of some of the isolated plants and the parts of the plant from which these were obtained lend support to their traditional use. Bulbine abyssinica and B. capitata yielded phenylanthraquinones, some of which were shown to possess strong antiplasmodial activity. In addition, these yielded isofuranonaphthoquinones, which were also found to be weakly antiplasmodial and antioxidant. Scilla nervosa yielded several known and novel homoisoflavoinds of the 3-benzylchroman-4-ones and 3-benzylidinechroman- 4-one type, as well as some stilbenoids. The homoisoflavonoids showed strong antitumor activity against various cancer cell lines. Rhus pyroides gave a novel bichalcone, which showed weak antifeedant activity, consistent with the observation by farmers that the plant was avoided by corn cricket. Results from investigated Dorstenia species originating from Cameroon, Ethiopia, and Tanzania yielded styrenes, coumarins, chalcones, and flavonoids. The chalcones and flavonoids showed various levels of prenylation or geranylation, and an observation made so far is that prenylated flavonoids are only found in Dorstenia species of African origin. The only example of a bis-geranylated chalcone is found in Dorstenia.

URI:

http://hdl.handle.net/10311/308

Files in this item: 1

Files in this item: 2

license.txt (1.998Kb)

Rotenoid deriva ... nstituents of the twig.pdf (3.786Mb)

Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives

Masesane, I.; Steel, P. (Elsevier Ltd; www.elsevier.com/locate/tetlet, June 21, 2004)

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Abstract:	The Diels-Alder adduct of ethyl (E)-3-nitroacrylate and furan provides a versatile template for the stereoselective synthesis of mono and dihydroxylated derivatives of 2-aminocyclohexanecarboxylic acid (ACHC). The hydroxylated ACHC derivatives can be considered to be useful building blocks for B-peptides.
URI:	http://hdl.handle.net/10311/235

Files in this item: 2

license.txt (1.998Kb)

Stereoselective routes to 3-hydroxy.pdf (721.3Kb)

Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl b-amino acid derivatives

Chola, J.; Masesane, I.B. (Elsevier Ltd. www.elsevier.com/ locate/tetlet, NaN, 2008)

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Abstract:	Stereoselective syntheses of racemic (1S,2R,3R,4R,5S,6R)- and (1S,2R,3R,4S,5S,6R)-3,4,5,6-tetrahydroxy derivatives of 2-aminocyclohexanecarboxylic acid have been achieved by a stereospecific Diels–Alder reaction between furan and maleic anhydride, a Curtius rearrangement and hydroxylation reactions.
URI:	http://hdl.handle.net/10311/325

Files in this item: 1

Stereoselective sythesis of 3.pdf (1.100Mb)

A study of the removal of heavy metals from aqueous solutions by Moringa oleifera seeds and amine-based ligand 1,4-bis[N,N-bis(2-picoyl)amino]butane

Obuseng, V.; Nareetsile, F.; Kwaambwa, H.M. (Elsevier Science Ltd, www.elsevier.com/locate/aca, NaN, 2012)

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Abstract:

Uptake for lead, copper, cadmium, nickel and manganese from aqueous solution using the Moringa oleifera seeds biomass (MOSB) and amine-based ligand (ABL) was investigated. Experiments on two synthetic multi-solute systems revealed that MOSB performed well in the biosorption and followed the decreasing orders Pb(II)>Cu(II)>Cd(II)>Ni(II)>Mn(II) and Zn(II)>Cu(II)>Ni(II). The general trend of the heavy metal ions uptake by the amine-based ligand followed decreased in the order Mn>Cd >Cu> Ni>Pb, which is the reverse trend for what was observed for MOSB. Comparing the single- and multi-metal solutions, there was no clear effect in the biosorption capacity of MOSB suggesting the presence of sufficient active binding sites for all metal ions studied. The MOSB performance is also not affected by pH in the range 3.5–8.

URI:

http://hdl.handle.net/10311/1039

Files in this item: 1

Obuseng_ACA_2012.pdf (886.0Kb)

Trace enrichment of metal ions in aquatic environments by Saccharomyces cerevisiae

Mapolelo, M.; Torto, N. (Elsevier; www.elsevier.com/locate/talanta, NaN, 2004)

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Abstract:

[Please note that chemical formulae do not display correctly in this abstract]. Sorption properties of baker's yeast cells, characterised as Saccharomyces cerevisiae were evaluated for trace enrichment of metal ions: Cd2+, Cr3+, Cr6+, Cu2+, Pb2+ and Zn2+ from aqueous environments. Metal concentration was determined by flame atomic absorption spectrometry (FAAS). Parameters affecting metal uptake such as solution pH, incubation time, amount of yeast biomass and effect of glucose concentration (energy source) were optimised. Further studies were carried out to evaluate the effects on metal uptake after treating yeast with glucose as well as with an organic solvent. The results showed that trace enrichment of the metals under study with yeast, depends upon the amount of yeast biomass, pH and incubation time. Treatment of yeast cells with 10-20mM glucose concentration enhanced metal uptake with exception to Cr6+, whose metal enrichment capacity decreased at glucose concentration of 60 mM. Of the investigated organic solvents THF and DMSO showed the highest and lowest capacity, respectively, to enhance metal uptake by yeast cells. Trace enrichment of metal ions from stream water, dam water, treated wastewater from a sewage plant and wastewater from an electroplating plant achieved enrichment factors (EF) varying from 1 to 98, without pre-treatment of the sample. pH adjustment further enhanced the EF for all samples. The results from these studies demonstrate that yeast is a viable trace metal enrichment media that can be used freely suspended in solution to achieve very high EF in aquatic environments.

URI:

http://hdl.handle.net/10311/156

Files in this item: 2

license.txt (1.998Kb)

mapolelotortonew.pdf (469.7Kb)

Two new anthraquinones from Gladiolus psittascinus

Ngamba, D.; Awouafack, M.; Tane, P.; Bezabih, M.; Abegaz, B. (Elsevier Ltd. www.elsevier.com/locate/biochemsyseco, NaN, 2007)

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Abstract:

Gladiolus psittascinus HOOK, an herbaceous plant, is propagated by its bulb. This onion-looking plant occurs in rocky places in western province of Cameroon. The bulbs are used to treat asthma, gonorrhoea, diabetes and intestinal parasites (Adjanohoun et al., 1990). The bulbs of G. psittascinus were collected in Dschang (West Province of Cameroon) in July 2005 and identified by Mr Francois Nana, a botanist at the National Herbarium, Yaounde where a voucher specimen (55925 HCN) is deposited. We report here the isolation and structural elucidation from the chloroform extract of two new anthraquinones namely: 1,6,7-trihydroxy-3-methoxy-8-methyl-anthraquinone (1) and 1-hydroxy-3,6,7-trimethoxy-8-methyl-anthraquinone (2) along with four known compounds. The structures of the compounds were elucidated by spectroscopic analysis, mainly, 1D and 2D NMR and by comparing their physical (mp) and spectroscopic (Table 1) data with those reported in the literature.

URI:

http://hdl.handle.net/10311/248

Files in this item: 4

license.txt (1.998Kb)

Two new anthraq ... Gladiolus psittascinus.pdf (2.394Mb)

Tylosema esculentum extractives and their bioactivity

Mazimba, O.; Majinda, R.R.; Modibedi, C.; Masesane, I.B.; Cencicˇ, A.; Chingwaru, W. (Elsevier Science Ltd, http://www.elsevier.com/locate/bmc, NaN, 2011)

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Abstract:

The investigation of Tylosema esculentum (Morama) husks, cotyledons, and tuber yielded griffonilide 2, compound 1, griffonin 3, gallic acid 4, protocatechuic acid 5, b-sitosterol 6, behenic acid 7, oleic acid 8, sucrose 9, 2-O-ethyl-a-D-glucopyranoside 10, kaempferol 11 and kaempferol-3-O-b-D-glucopyranoside 12. The structures of the isolates were determined by NMR, HR-TOF EIMS, IR and UV–vis spectroscopy, and by comparison with literature data. The husk EtOAc and n-butanol extracts demonstrated >90% DPPH radical scavenging activity at concentrations of 25, 50 and 250 lg/mL. Furthermore the husk extracts showed higher total phenolic content (233 mg GAE/g). The extractives exhibited minimum inhibitory quantities of 50–100 lg or no activity against Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Pseudomonas aeruginosa and Candida albicans. The tuber extracts were inactive against Caco-2 and Hela cell lines, while the husk extracts showed low activity against Caco-2 and Vero cell line with IC50 values >400 lg/mL. The GC–MS analysis showed the beans and tuber non-polar (n-hexane) extracts major constituents as fatty acids.

URI:

http://hdl.handle.net/10311/1029

Files in this item: 1

Mazimba_BMC_2011.pdf (698.8Kb)

An unexpected 1,2-hydride shift in phosphoric acid-promoted cyclodimerization of styrene oxides under solvent-free conditions. A synthetic route towards 2,4-disubstituted 1,3-dioxolanes

Mazimba, O.; Majinda, R.R.; Masesane, I.B. (Elsevier Science Ltd, http://www.elsevier.com/locate/tetlet, NaN, 2009)

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A 1,2-hydride shift in the phosphoric acid-promoted cyclodimerization of styrene oxide and its chloro derivatives under solvent-free conditions leading to 2,4-disubstituted 1,3-dioxolanes is described. Methoxy substituents on the aromatic ring of the styrene oxide prevent the 1,2-hydride shift reaction leading to substituted 1,4-dioxanes. A possible mechanism for the formation of the 1,3-dioxolanes is proposed.

URI:

http://hdl.handle.net/10311/1026

Files in this item: 1

Masesane_TL_2009.pdf (246.5Kb)

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