Affecting surface chirality via multicomponent adsorption of chiral and achiral molecules

Here we report on the apparent reduction in surface chirality upon co-assembling a chiral and achiral molecule into a physisorbed self-assembled monolayer at the liquid/solid interface as revealed by scanning tunneling microscopy (STM). Chiral OPV with achiral thymine gives rise to surface-confined supramolecular diastereomers

Institutions and governance of communal rangelands in South Africa

The creation of local institutions with a mandate over land access and control is seen as a prerequisite for successful decentralisation of land tenure and effective local resource management in sub-Saharan Africa. However, with land tenure reform in South Africa currently at a state of legislative impasse, real uncertainty now exists over land rights and governance of rangeland in many communal areas. This paper draws on case study material from Eastern Cape province to illustrate how this ongoing uncertainty has resulted in the operation of a range of traditional authority and civil society institutions in different communal areas with varying degrees of legitimate authority over land administration and highly variable performance in managing rangeland resources. Collective management of rangeland resources seems most difficult in environments where land rights are contested because of the coexistence of traditional leaders and civil society institutions. On this basis an approach to tenure reform is advocated, which vests all powers over local land administration in democratically elected and accountable civil society institutions. Some successful examples of this already exist and might serve to guide policy formation, which must be flexible enough to accommodate collective management approaches that emphasise cooperation both within and between communities.Keywords: common property, land tenure, natural resource management, traditional leadersAfrican Journal of Range & Forage Science 2013, 30(1&2): 77–8

Cross-Location Analysis of the Impact of Household Socioeconomic Status on Participation in Urban and Peri-Urban Agriculture in West Africa

This study explores the relation between household socioeconomic status (SES) and participation in urban and periurban agriculture (UPA) in three West African cities. We used a structured questionnaire to survey 700 randomly selected households: 250 in Kano, Nigeria, 250 in Bobo Dioulasso, Burkina Faso, and 200 in Sikasso, Mali. Multiple correspondence analysis was applied on household asset variables to create an index of assets which was used as a proxy for household SES. The results showed no significant differences in households’ rate of participation in UPA across socioeconomic groups. Participation in UPA was rather significantly (P < 0.001) and positively related to household size. Interestingly, the analysis revealed that field crop cultivation and gardening were more common among households in the low and medium SES groups while those in the high SES group were more likely to keep livestock

Deagrarianisation and forest revegetation in a biodiversity hotspot on the Wild Coast, South Africa

Deagraianisation is a worldwide phenomenon with widespread social, ecological and economic effects yet with little consensus on the local or higher level causes. There have been contested views on the causes and consequences of deagrarianisation on South Africa’s Wild Coast, which is an international biodiversity hotspot. Using GIS, household interviews and ecological sampling, we compared the perspectives of current and former cultivators as to why some have abandoned farming, whilst also tracking the uses and woody plant cover and composition of fields abandoned at different periods. The GIS analysis showed that field abandonment had been ongoing over several decades, with a decline from 12.5 % field cover in 1961 to 2.7 % in 2009. The area of forests and woodlands almost doubled in the corresponding period. There was a distinct peak in field abandonment during the time of political transition at the national level in the early 1990s. This political change led to a decrease in government support for livestock farming, which in turn resulted in reduced animal draught power at the household and community level, and hence reduced cropping. The study showed it is largely the wealthier households that have remained in arable agriculture and that the poorer households have abandoned farming. The abandoned fields show a distinct trend of increasing woody biomass and species richness with length of time since abandonment, with approximately three woody plant species added per decade. Most local respondents dislike the increases in forest and woodland extent and density because of anxiety about wild animals causing harm to crops and even humans, and the loss of an agricultural identity to livelihoods and the landscape

Asymmetric noncovalent synthesis of self-assembled one-dimensional stacks by a chiral supramolecular auxiliary approach

Stereoselective noncovalent synthesis of one-dimensional helical self-assembled stacks of achiral oligo(p-phenylenevinylene) ureidotriazine (AOPV3) monomers is obtained by a chiral supramolecular auxiliary approach. The racemic mixture of helical stacks of achiral AOPV3 molecules is converted into homochiral helical stacks, as shown by both spectroscopic measurements and molecular modeling simulations. The conversion is promoted by an orthogonal two-point ion-pair interaction with the chiral auxiliary dibenzoyl tartaric acid (d- or l-TA) molecules, which biases the angle population distribution and thereby the stack helicity. The induced preferred helicity is maintained by the OPV stacks even after the removal of the chiral auxiliary by extraction with ethylenediamine (EDA), due to the kinetic stability of the OPV stacks at room temperature. Spectroscopic probing of the helical self-assembly and the racemization process of these p-conjugated OPV chromophores shed further light into the mechanistic pathways of this chiral asymmetric noncovalent synthesis and the kinetic stability of the stacks produced. The racemization of the stacks follows first-order kinetics and no switch in mechanism is observed as a result of a temperature change; therefore, a racemization via disassembly assembly is proposed. Remarkably, the preferred helicity of the stacks of achiral AOPV3 can be retained almost completely after a heating–cooling cycle where the stacks first partially depolymerize and then polymerize again with the still existing stacks being the seeds for self-assembly of achiral AOPV3. Only after a fully dissociated state is obtained at high temperatures, the optical activity of the supramolecular stack self-assembled at room temperature is lost

Asymmetric noncovalent synthesis of self-assembled one-dimensional stacks by a chiral supramolecular auxiliary approach

Stereoselective noncovalent synthesis of one-dimensional helical self-assembled stacks of achiral oligo(p-phenylenevinylene) ureidotriazine (AOPV3) monomers is obtained by a chiral supramolecular auxiliary approach. The racemic mixture of helical stacks of achiral AOPV3 molecules is converted into homochiral helical stacks, as shown by both spectroscopic measurements and molecular modeling simulations. The conversion is promoted by an orthogonal two-point ion-pair interaction with the chiral auxiliary dibenzoyl tartaric acid (d- or l-TA) molecules, which biases the angle population distribution and thereby the stack helicity. The induced preferred helicity is maintained by the OPV stacks even after the removal of the chiral auxiliary by extraction with ethylenediamine (EDA), due to the kinetic stability of the OPV stacks at room temperature. Spectroscopic probing of the helical self-assembly and the racemization process of these p-conjugated OPV chromophores shed further light into the mechanistic pathways of this chiral asymmetric noncovalent synthesis and the kinetic stability of the stacks produced. The racemization of the stacks follows first-order kinetics and no switch in mechanism is observed as a result of a temperature change; therefore, a racemization via disassembly assembly is proposed. Remarkably, the preferred helicity of the stacks of achiral AOPV3 can be retained almost completely after a heating–cooling cycle where the stacks first partially depolymerize and then polymerize again with the still existing stacks being the seeds for self-assembly of achiral AOPV3. Only after a fully dissociated state is obtained at high temperatures, the optical activity of the supramolecular stack self-assembled at room temperature is lost

Asymmetric noncovalent synthesis of self-assembled one-dimensional stacks by a chiral supramolecular auxiliary approach

Stereoselective noncovalent synthesis of one-dimensional helical self-assembled stacks of achiral oligo(p-phenylenevinylene) ureidotriazine (AOPV3) monomers is obtained by a chiral supramolecular auxiliary approach. The racemic mixture of helical stacks of achiral AOPV3 molecules is converted into homochiral helical stacks, as shown by both spectroscopic measurements and molecular modeling simulations. The conversion is promoted by an orthogonal two-point ion-pair interaction with the chiral auxiliary dibenzoyl tartaric acid (d- or l-TA) molecules, which biases the angle population distribution and thereby the stack helicity. The induced preferred helicity is maintained by the OPV stacks even after the removal of the chiral auxiliary by extraction with ethylenediamine (EDA), due to the kinetic stability of the OPV stacks at room temperature. Spectroscopic probing of the helical self-assembly and the racemization process of these p-conjugated OPV chromophores shed further light into the mechanistic pathways of this chiral asymmetric noncovalent synthesis and the kinetic stability of the stacks produced. The racemization of the stacks follows first-order kinetics and no switch in mechanism is observed as a result of a temperature change; therefore, a racemization via disassembly assembly is proposed. Remarkably, the preferred helicity of the stacks of achiral AOPV3 can be retained almost completely after a heating–cooling cycle where the stacks first partially depolymerize and then polymerize again with the still existing stacks being the seeds for self-assembly of achiral AOPV3. Only after a fully dissociated state is obtained at high temperatures, the optical activity of the supramolecular stack self-assembled at room temperature is lost

Superexchange-mediated electronic energy transfer in a model dyad

On the basis of time-dependent density functional theory (TD-DFT) calculations coupled to the polarizable continuum model (PCM) and single molecule spectroscopic studies, we provide a detailed investigation of excitation energy transfer within a model bi-chromophoric system where a perylene monoimide (PMI) donor is bridged to a terrylene diimide (TDI) acceptor through a ladder-type pentaphenylene (pPh) spacer. We find that the electronic excitation on the PMI donor significantly extends over the bridge giving rise to a partial charge transfer character and inducing a B3-fold increase in the electronic interaction between the chromophores, which explains the failure of the Forster model in reproducing the observed energy migration rates when treating PMI as the donor. However, despite an increased charge transfer contribution in the effective donor state, the increase in solvent polarity is not accompanied by an enhancement in the electronic coupling between the subunits, which is rationalized from a detailed analysis of the excited-state wavefunctions