The use of GIS in Brownfield redevelopment

In recent years, the issue of Brownfield site development - the re-use of previously used urban land - has gained a significant place in the planning agenda. However, not all Brownfield sites are derelict or contaminated land, some are significant as environmental amenities - be it part of wider ecosystem or a green area for the local population. The growing concern to include environmental aspects into the public debate have lead the Environment Agency, the Jackson Environment Institute and the Centre for Advanced Spatial Analysis to commission a short term pilot study to evaluate the contribution of a GIS for decision support and for "discussion support".In this paper, we describe how the state-of-the-art in geographic information (GI) and GI Science (GISc) can be used in a short term and limited project to achieve a practical and usable system. We are drawing on developments in information availability, as made accessible through the World Wide Web and research themes in GISc ranging from Multimedia GIS to Public Participation GIS

“Cross” Supermicelles via the Hierarchical Assembly of Amphiphilic Cylindrical Triblock Comicelles

Self-assembled “cross” architectures are well-known in biological systems (as illustrated by chromosomes, for example); however, comparable synthetic structures are extremely rare. Herein we report an in depth study of the hierarchical assembly of the amphiphilic cylindrical P–H–P triblock comicelles with polar (P) coronal ends and a hydrophobic (H) central periphery in a selective solvent for the terminal segments which allows access to “cross” supermicelles under certain conditions. Well-defined P–H–P triblock comicelles M­(PFS-<i>b</i>-PtBA)-<i>b</i>-M­(PFS-<i>b</i>-PDMS)-<i>b</i>-M­(PFS-<i>b</i>-PtBA) (M = micelle segment, PFS = polyferrocenyldimethylsilane, PtBA = poly­(<i>tert</i>-butyl acrylate), and PDMS = polydimethylsiloxane) were created by the living crystallization-driven self-assembly (CDSA) method. By manipulating two factors in the supermicelles, namely the H segment-solvent interfacial energy (through the central H segment length, <i>L</i>₁) and coronal steric effects (via the PtBA corona chain length in the P segment, <i>L</i>₂ related to the degree of polymerization DP₂) the aggregation of the triblock comicelles could be finely tuned. This allowed a phase-diagram to be constructed that can be extended to other triblock comicelles with different coronas on the central or end segment where “cross” supermicelles were exclusively formed under predicted conditions. Laser scanning confocal microscopy (LSCM) analysis of dye-labeled “cross” supermicelles, and block “cross” supermicelles formed by addition of a different unimer to the arm termini, provided complementary characterization to transmission electron microscopy (TEM) and dynamic light scattering (DLS) and confirmed the existence of these “cross” supermicelles as kinetically stable, micron-size colloidally stable structures in solution

Dimensional control and morphological transformations of supramolecular polymeric nanofibers based on cofacially-stacked planar amphiphilic platinum(II) complexes

Square-planar platinum­(II) complexes often stack cofacially to yield supramolecular fiber-like structures with interesting photophysical properties. However, control over fiber dimensions and the resulting colloidal stability is limited. We report the self-assembly of amphiphilic Pt­(II) complexes with solubilizing ancillary ligands based on polyethylene glycol [PEG_<i>n</i>, where <i>n</i> = 16, 12, 7]. The complex with the longest solubilizing PEG ligand, <b>Pt-PEG</b>_<b>16</b>, self-assembled to form polydisperse one-dimensional (1D) nanofibers (diameters <5 nm). Sonication led to short seeds which, on addition of further molecularly dissolved <b>Pt-PEG</b>_<b>16</b> complex, underwent elongation in a “living supramolecular polymerization” process to yield relatively uniform fibers of length up to <i>ca</i>. 400 nm. The fiber lengths were dependent on the <b>Pt-PEG</b>_<b>16</b> complex to seed mass ratio in a manner analogous to a living covalent polymerization of molecular monomers. Moreover, the fiber lengths were unchanged in solution after 1 week and were therefore “static” with respect to interfiber exchange processes on this time scale. In contrast, similarly formed near-uniform fibers of <b>Pt-PEG</b>_<b>12</b> exhibited dynamic behavior that led to broadening of the length distribution within 48 h. After aging for 4 weeks in solution, <b>Pt-PEG</b>_<b>12</b> fibers partially evolved into 2D platelets. Furthermore, self-assembly of <b>Pt-PEG</b>_<b>7</b> yielded only transient fibers which rapidly evolved into 2D platelets. On addition of further fiber-forming Pt complex (<b>Pt-PEG</b>_<b>16</b>), the platelets formed assemblies <i>via</i> the growth of fibers selectively from their short edges. Our studies demonstrate that when interfiber dynamic exchange is suppressed, dimensional control and hierarchical structure formation are possible for supramolecular polymers through the use of kinetically controlled seeded growth methods

On Chamœmeles coriacea and Sempervivum glutinosum

Volume: 16Start Page: 393End Page: 39

Long-range exciton transport in conjugated polymer nanofibers prepared by seeded growth.

Easily processed materials with the ability to transport excitons over length scales of more than 100 nanometers are highly desirable for a range of light-harvesting and optoelectronic devices. We describe the preparation of organic semiconducting nanofibers comprising a crystalline poly(di-n-hexylfluorene) core and a solvated, segmented corona consisting of polyethylene glycol in the center and polythiophene at the ends. These nanofibers exhibit exciton transfer from the core to the lower-energy polythiophene coronas in the end blocks, which occurs in the direction of the interchain π-π stacking with very long diffusion lengths (>200 nanometers) and a large diffusion coefficient (0.5 square centimeters per second). This is made possible by the uniform exciton energetic landscape created by the well-ordered, crystalline nanofiber core

Long-range exciton transport in conjugated polymer nanofibers prepared by seeded growth.

Easily processed materials with the ability to transport excitons over length scales of more than 100 nanometers are highly desirable for a range of light-harvesting and optoelectronic devices. We describe the preparation of organic semiconducting nanofibers comprising a crystalline poly(di-n-hexylfluorene) core and a solvated, segmented corona consisting of polyethylene glycol in the center and polythiophene at the ends. These nanofibers exhibit exciton transfer from the core to the lower-energy polythiophene coronas in the end blocks, which occurs in the direction of the interchain π-π stacking with very long diffusion lengths (>200 nanometers) and a large diffusion coefficient (0.5 square centimeters per second). This is made possible by the uniform exciton energetic landscape created by the well-ordered, crystalline nanofiber core