14 research outputs found
Gender essentialism and occupational segregation in insolvency practice
Advances towards egalitarianism in professional recruitment may be offset by processes of occupational re-segregation. Drawing on gender theory this paper investigates horizontal segregation in the UK insolvency profession, as revealed through the lived experiences of female and male practitioners. It is shown that horizontal segregation pervades at different levels of practice and is undergirded by various elements of gender essentialism. Physical essentialism explains why insolvency practice has been traditionally gendered male. Interactional essentialism combines with the management of work-life balance to define the subfields of corporate and personal insolvency as masculine and feminine respectively. Gender essentialist assumptions also pervade the distribution of roles and the allocation of work tasks. Networks are identified as arenas for the reproduction and perpetuation of occupational segregation. The findings indicate the continuing potency of gender in everyday professional life, the limitations of diversity-orientated policies and the complexities of formulating transformative agendas
ChemInform Abstract: Synthesis and Structural Characterization of the Anion Nido-[B8H11]-, and New Insights into the Structures of Other Octaborane Species
The life and works of Dr John Bastwick (1595-1654)
Available from British Library Document Supply Centre-DSC:DX216770 / BLDSC - British Library Document Supply CentreSIGLEGBUnited Kingdo
Synthesis and structural characterisation of the anion nido-[B8H11](-), and new insights into the structures of other octaborane species
Cyclic localization of actin and its relationship to junctional complexes in maturation ameloblasts of the rat incisor
Macropolyhedral boron-containing cluster chemistry. The reversible disassembly and reassembly of the hexagonal pyramidal {B7} feature in the [S2B18H19]â anion
Hydroboration of Phosphaalkynes by HB(C 6
The hydroboration of phosphaalkynes with Piersâ borane (HB(C6F5)2) generated unusual phosphaalkenylboranes [RCH=PB(C6F5)2]2 that persisted as dimers in both solution and the solid state. These P2B2 heterocycles underwent ring opening when subjected to nucleophiles, such as pyridine and tert-butylisocyanide, to yield monomeric phosphaalkenylborane adducts RCH=PB(C6F5)2 (L). DFT calculations were performed to probe the nature of the interaction of phosphaalkynes with boranes