Burrow utilization by springhares (Pedetescapensis) in the Eastern Cape, South Africa
- Authors: Peinke, D M , Brown, C R
- Date: 2005
- Language: English
- Type: Article
- Identifier: vital:6962 , http://hdl.handle.net/10962/d1012025
- Description: The use of burrows by springhares was investigated in the Eastern Cape, South Africa using radio telemetry. Springhares utilized 4–27 different burrows scattered over areas ranging from 0.6–28.5 ha, with maximum distances of 170–1000 m between burrows. Springhares frequently changed burrows, seldom spending more than a few consecutive days in each, unless rearing young. The number of burrows used by individuals was correlated with the length of time they were tracked and, even after a year, some individuals were still occupying burrows previously unused by them. Males and females did not differ significantly in the mean number of burrows used, the mean area over which these were distributed, or the mean maximum distance between burrows. Springhares were generally solitary and occupied burrows were, with few exceptions, apparently avoided by conspecifics.
- Full Text:
- Date Issued: 2005
- Authors: Peinke, D M , Brown, C R
- Date: 2005
- Language: English
- Type: Article
- Identifier: vital:6962 , http://hdl.handle.net/10962/d1012025
- Description: The use of burrows by springhares was investigated in the Eastern Cape, South Africa using radio telemetry. Springhares utilized 4–27 different burrows scattered over areas ranging from 0.6–28.5 ha, with maximum distances of 170–1000 m between burrows. Springhares frequently changed burrows, seldom spending more than a few consecutive days in each, unless rearing young. The number of burrows used by individuals was correlated with the length of time they were tracked and, even after a year, some individuals were still occupying burrows previously unused by them. Males and females did not differ significantly in the mean number of burrows used, the mean area over which these were distributed, or the mean maximum distance between burrows. Springhares were generally solitary and occupied burrows were, with few exceptions, apparently avoided by conspecifics.
- Full Text:
- Date Issued: 2005
Effects of number of ring substituents on the physicochemical properties of zinc aminophenoxy phthalocyanine-single walled carbon nanotube conjugate
- Ogbodu, Racheal O, Nyokong, Tebello
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7319 , http://hdl.handle.net/10962/d1020564
- Description: This work reports on the linking of zinc monoaminophenoxy (ZnMAPPc) or zinc tetraaminophenoxy phthalocyanine (ZnTAPPc) complexes to single walled carbon nanotubes (SWCNTs) through either covalent or non-covalent (adsorption) bonding. The functionalized complexes showed better thermal stability when compared to the SWCNT-COOH, ZnMAPPc and ZnTAPPc alone as confirmed by thermogravimetric analyses. The covalently linked ZnMAPc-SWCNT showed higher electron transfer rate constant and photoinduced electron efficiency when compared to adsorbed complexes. ZnMAPPc-SWCNT complexes (linked and adsorbed) showed better photophysical and photochemical properties when compared to ZnTAPPc-SWCNT complexes. The triplet, singlet oxygen and florescence quantum yields of ZnMAPPc (or ZnTAPPc) decrease upon linking or adsorption onto SWCNTs. , Original publication is available at http://dx.doi.org/10.1016/j.jphotochem.2013.09.015
- Full Text: false
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7319 , http://hdl.handle.net/10962/d1020564
- Description: This work reports on the linking of zinc monoaminophenoxy (ZnMAPPc) or zinc tetraaminophenoxy phthalocyanine (ZnTAPPc) complexes to single walled carbon nanotubes (SWCNTs) through either covalent or non-covalent (adsorption) bonding. The functionalized complexes showed better thermal stability when compared to the SWCNT-COOH, ZnMAPPc and ZnTAPPc alone as confirmed by thermogravimetric analyses. The covalently linked ZnMAPc-SWCNT showed higher electron transfer rate constant and photoinduced electron efficiency when compared to adsorbed complexes. ZnMAPPc-SWCNT complexes (linked and adsorbed) showed better photophysical and photochemical properties when compared to ZnTAPPc-SWCNT complexes. The triplet, singlet oxygen and florescence quantum yields of ZnMAPPc (or ZnTAPPc) decrease upon linking or adsorption onto SWCNTs. , Original publication is available at http://dx.doi.org/10.1016/j.jphotochem.2013.09.015
- Full Text: false
Enhanced triplet state parameters for zinc carboxy phenoxy phthalocyanine following conjugation to ascorbic acid: effects of adsorption on single walled carbon nanotubes
- Ogbodu, Racheal O, Nyokong, Tebello
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7265 , http://hdl.handle.net/10962/d1020274
- Description: Zinc phthalocyanine bearing four ascorbic acid units (formed via ester bond between zinc carboxy phenoxy phthalocyanines and ascorbic acid) was synthesized and characterized using different spectroscopic methods. The complex (with or without ascorbic acid) was further adsorbed onto single walled carbon nanotubes (SWCNTs) and further characterized using Raman spectroscopy, X-ray diffractometry, transmission electron microscopy and thermogravimetric analysis. The photophysical properties of the complexes were studied. The synthesized complex showed better photophysical properties when compared to the carboxy phenoxy phthalocyanines alone, this is evident in the increase of the triplet quantum yields (ΦT), triplet life-times (τT) and singlet oxygen quantum yields (ΦΔ). The zinc phthalocyanines bearing ascorbic acid showed improved triplet life-times even in the presence of SWCNTs. , Original publication is available at http://dx.doi.org/10.1016/j.poly.2015.01.032
- Full Text: false
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7265 , http://hdl.handle.net/10962/d1020274
- Description: Zinc phthalocyanine bearing four ascorbic acid units (formed via ester bond between zinc carboxy phenoxy phthalocyanines and ascorbic acid) was synthesized and characterized using different spectroscopic methods. The complex (with or without ascorbic acid) was further adsorbed onto single walled carbon nanotubes (SWCNTs) and further characterized using Raman spectroscopy, X-ray diffractometry, transmission electron microscopy and thermogravimetric analysis. The photophysical properties of the complexes were studied. The synthesized complex showed better photophysical properties when compared to the carboxy phenoxy phthalocyanines alone, this is evident in the increase of the triplet quantum yields (ΦT), triplet life-times (τT) and singlet oxygen quantum yields (ΦΔ). The zinc phthalocyanines bearing ascorbic acid showed improved triplet life-times even in the presence of SWCNTs. , Original publication is available at http://dx.doi.org/10.1016/j.poly.2015.01.032
- Full Text: false
Photophysical and non-linear optical behavior of novel tetra alkynyl terminated indium phthalocyanines: Effects of the carbon chain length
- Bankole, Owolabi M, Britton, Jonathan, Nyokong, Tebello
- Authors: Bankole, Owolabi M , Britton, Jonathan , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7262 , http://hdl.handle.net/10962/d1020271
- Description: We report on the synthesis, photophysical and nonlinear optical behavior of tetra-substituted alkynyl indium phthalocyanine complexes (3a and 3b). Both complexes showed large triplet quantum yields. Nonlinear optical properties were also evaluated for the two complexes at a wavelength of 532 nm using nanosecond Z-scan technique in dimethylsulfoxide. We observed two-photon absorption (2PA) and strong reverse saturable absorption (RSA) as the dominant mechanisms at nanosecond laser excitation. The underlining 2PA and observed RSA were subjected to further scrutiny by comparing the analytical absorption model to the transmittance optical absorption theory. The theoretical results were in good agreement to the observed RSA and the 2PA mechanism. Large two-photon absorption cross-section (1.29 × 10−42 and 1.15 × 10−42 cm4 s/photon), third-order susceptibility (2.10 × 10−14 and 2.15 × 10−14 esu) and hyperpolarizability (2.70 × 10−32 and 3.19 × 10−32 esu) were estimated for complex 3a and 3b, respectively. , Original publication is available at http://dx.doi.org/10.1016/j.poly.2014.12.020
- Full Text: false
- Authors: Bankole, Owolabi M , Britton, Jonathan , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7262 , http://hdl.handle.net/10962/d1020271
- Description: We report on the synthesis, photophysical and nonlinear optical behavior of tetra-substituted alkynyl indium phthalocyanine complexes (3a and 3b). Both complexes showed large triplet quantum yields. Nonlinear optical properties were also evaluated for the two complexes at a wavelength of 532 nm using nanosecond Z-scan technique in dimethylsulfoxide. We observed two-photon absorption (2PA) and strong reverse saturable absorption (RSA) as the dominant mechanisms at nanosecond laser excitation. The underlining 2PA and observed RSA were subjected to further scrutiny by comparing the analytical absorption model to the transmittance optical absorption theory. The theoretical results were in good agreement to the observed RSA and the 2PA mechanism. Large two-photon absorption cross-section (1.29 × 10−42 and 1.15 × 10−42 cm4 s/photon), third-order susceptibility (2.10 × 10−14 and 2.15 × 10−14 esu) and hyperpolarizability (2.70 × 10−32 and 3.19 × 10−32 esu) were estimated for complex 3a and 3b, respectively. , Original publication is available at http://dx.doi.org/10.1016/j.poly.2014.12.020
- Full Text: false
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