An argument for VP coordination: scene-setting coordination and weak islands
- Authors: De Vos, Mark A
- Date: 2009
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/469371 , vital:77236 , https://doi.org/10.2989/SALALS.2009.27.1.1.749
- Description: This article provides a minimalist analysis of a novel type of weak island that has not been discussed in the literature until now. The island is a subtype of extraction from asymmetric coordination islands in violation of the across-the-board constraint. The islands in question are characterised by being weak islands for certain types of adjunct extraction, and by being discontinuous – XP coordination. This article demonstrates the properties of this curious construction type and proposes the first analysis to date. It is argued that this is an instance of VP coordination and that this configuration allows the possibility of high merger of direct objects in a constrained fashion.
- Full Text:
- Authors: De Vos, Mark A
- Date: 2009
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/469371 , vital:77236 , https://doi.org/10.2989/SALALS.2009.27.1.1.749
- Description: This article provides a minimalist analysis of a novel type of weak island that has not been discussed in the literature until now. The island is a subtype of extraction from asymmetric coordination islands in violation of the across-the-board constraint. The islands in question are characterised by being weak islands for certain types of adjunct extraction, and by being discontinuous – XP coordination. This article demonstrates the properties of this curious construction type and proposes the first analysis to date. It is argued that this is an instance of VP coordination and that this configuration allows the possibility of high merger of direct objects in a constrained fashion.
- Full Text:
Peacekeeping in Africa: problems and prospects
- Authors: Juma, Laurence
- Date: 2009
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/129113 , vital:36219 , https://heinonline.org/HOL/P?h=hein.journals/unbotslj9amp;i=3
- Description: Against the background of an expanded need for peacekeeping, the complexity that its programmes entail, and the belief that it will endure for a long time to come, this article discusses the propriety of international peacekeeping operations, its inherent features and weaknesses in creating or preserving peace, and the role that regional organisations play, or should play, in its enhancement.
- Full Text: false
- Authors: Juma, Laurence
- Date: 2009
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/129113 , vital:36219 , https://heinonline.org/HOL/P?h=hein.journals/unbotslj9amp;i=3
- Description: Against the background of an expanded need for peacekeeping, the complexity that its programmes entail, and the belief that it will endure for a long time to come, this article discusses the propriety of international peacekeeping operations, its inherent features and weaknesses in creating or preserving peace, and the role that regional organisations play, or should play, in its enhancement.
- Full Text: false
Synthesis and Pd(II) binding studies of octasubstituted alkyl thio derivatised phthalocyanines
- Ogunbayo, T B, Nyokong, Tebello
- Authors: Ogunbayo, T B , Nyokong, Tebello
- Date: 2009
- Language: English
- Type: Article
- Identifier: vital:6587 , http://hdl.handle.net/10962/d1004170
- Description: Synthesis and characterization of non-peripherally (4,5) and peripherally (6,7) substituted metal free and Pd octapentylthiophthalocyanine and coordination of palladium ions to these Pcs are reported. The unmetalated complexes (4 and 6) show Pd coordination at the central metal and at the ring. The number of Pd ions bound to complex 4 were found to be five and to complex 6 were three. The equilibrium constant for the binding of Pd to complexes 4 was lower (K = 1.2 × 109 dm3 mol−1) than for complex 6 (K = 5.7 × 1010 dm3 mol−1).
- Full Text:
- Authors: Ogunbayo, T B , Nyokong, Tebello
- Date: 2009
- Language: English
- Type: Article
- Identifier: vital:6587 , http://hdl.handle.net/10962/d1004170
- Description: Synthesis and characterization of non-peripherally (4,5) and peripherally (6,7) substituted metal free and Pd octapentylthiophthalocyanine and coordination of palladium ions to these Pcs are reported. The unmetalated complexes (4 and 6) show Pd coordination at the central metal and at the ring. The number of Pd ions bound to complex 4 were found to be five and to complex 6 were three. The equilibrium constant for the binding of Pd to complexes 4 was lower (K = 1.2 × 109 dm3 mol−1) than for complex 6 (K = 5.7 × 1010 dm3 mol−1).
- Full Text:
Synthesis, spectroscopic and electrochemical properties of manganese, nickel and iron octakis-(2-diethylaminoethanethiol)-phthalocyanine
- Adebayo, A I, Nyokong, Tebello
- Authors: Adebayo, A I , Nyokong, Tebello
- Date: 2009
- Language: English
- Type: Article
- Identifier: vital:6563 , http://hdl.handle.net/10962/d1004122
- Description: The syntheses, spectroscopic and electrochemical properties of manganese (3), nickel (4) and iron (5) phthalocyanine complexes, octa-substituted at the peripheral positions with diethlyaminoethanethiol substituent, are reported. The electrochemistry of these complexes and the corresponding cobalt complex (6) are reported. Complex 3 showed two reversible reduction couples attributed to the MnIIIPc−2/MnIIPc−2 (E½ = −0.12 V versus Ag|AgCl) and MnIIPc−2/MnIIPc−3 (E½ = −0.82 V versus Ag|AgCl) species. Two ring-based reduction couples were also observed for complex 4. Two reduction couples, assigned to the FeIIPc−2/FeIPc−2 (E½ = −0.35 V versus Ag|AgCl) and FeIPc−2/FeIPc−3 (E½ = −0.96 V versus Ag|AgCl) species, and an oxidation couple, attributed to FeIIIPc−2/FeIIPc−2 (E½ = 0.26 V versus Ag|AgCl) species, were observed. For complex 6, two reductions and one oxidation were also observed with the potential range of 1.2 to −1.8 V versus Ag|AgCl Spectroelectrochemical studies were used to confirm some of the assigned processes.
- Full Text:
- Authors: Adebayo, A I , Nyokong, Tebello
- Date: 2009
- Language: English
- Type: Article
- Identifier: vital:6563 , http://hdl.handle.net/10962/d1004122
- Description: The syntheses, spectroscopic and electrochemical properties of manganese (3), nickel (4) and iron (5) phthalocyanine complexes, octa-substituted at the peripheral positions with diethlyaminoethanethiol substituent, are reported. The electrochemistry of these complexes and the corresponding cobalt complex (6) are reported. Complex 3 showed two reversible reduction couples attributed to the MnIIIPc−2/MnIIPc−2 (E½ = −0.12 V versus Ag|AgCl) and MnIIPc−2/MnIIPc−3 (E½ = −0.82 V versus Ag|AgCl) species. Two ring-based reduction couples were also observed for complex 4. Two reduction couples, assigned to the FeIIPc−2/FeIPc−2 (E½ = −0.35 V versus Ag|AgCl) and FeIPc−2/FeIPc−3 (E½ = −0.96 V versus Ag|AgCl) species, and an oxidation couple, attributed to FeIIIPc−2/FeIIPc−2 (E½ = 0.26 V versus Ag|AgCl) species, were observed. For complex 6, two reductions and one oxidation were also observed with the potential range of 1.2 to −1.8 V versus Ag|AgCl Spectroelectrochemical studies were used to confirm some of the assigned processes.
- Full Text:
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