360 research outputs found

    Homoleptic metal complexes of 4'-(5-pyrimidinyl)-2,2':6',2''-terpyridine : tetrafurcated expanded ligands

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    With iron(II) and ruthenium(II), 4`-(5-pyrimidinyl)-2,2`: 6`,2 ``-terpyridine (L) preferentially coordinates through the tpy domain to give octahedral [ML2](2+) (M Fe, Ru) complexes. Treatment of [RuL2][PF6](2) with CuCl2 center dot 2H(2)O leads to [Ru(2)(2)][CuCl2(OH2)][CuCl3]Cl center dot 3MeCN center dot 7H(2)O(n) which exhibits a two-dimensional coordination network with copper(II) centres interconnecting [RuL2](2+) motifs. Magnetic susceptibility data for the material are consistent with a one-dimensional S = 1/2 antiferromagnetic chain

    Structural diversity in the reactions of 4 '-(pyridyl)-2,2 ':6 ',2 ''-terpyridine ligands and bis{4 '-(4-pyridyl)-2,2 ':6 ',2 ''-terpyridine}iron(II) with copper(II) salts

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    We have demonstrated that treatment of [Fe(1)(2)](2+) (1 = 4'-(4-pyridyl)-2,2':6',2 ''-terpyridine) with an excess of CuCl2 center dot 2H(2)O leads to competition between coordination of copper(II) by the pendant pyridine donors in [Fe(1)(2)](2+), and transfer of ligand 1 from iron(II) to copper(II) to yield [{Cl3Cu(mu-1)Fe(mu-1)}(2)CuCl2(OH2)(2)]Cl-2 center dot 4H(2)O and [Cu(H1)Cl-2]Cl center dot 4H(2)O, respectively. Direct reaction of 1 with CuCl2 center dot 2H(2)O and variation in crystallization conditions results in the formation of either monomeric or polymeric complexes: [Cu(1)Cl-2]center dot 4.75H(2)O, [Cu(1)Cl-2]center dot H2O center dot MeOH and [Cu(1)Cl-2 center dot 2H(2)O](n). The reaction of 1 with Cu(NO3)(2)center dot 3H(2)O gives the coordination polymer [Cu(1)(ONO2)(2)center dot H2O](n). Magnetic data for [Cu(1)Cl-2 center dot 2H(2)O](n) and [Cu(1)(ONO2)(2)center dot H2O](n) are consistent with antiferromagnetically- coupled chains. Reactions of CuCl2 center dot 2H(2)O with ligands 2 and 3 (2 = 4'-(3-pyridyl)-2,2':6',2 ''-terpyridine, 3 = 4'-(2-pyridyl)-2,2':6',2 ''-terpyridine) lead to monomeric complexes. With the exception of [Cu(3)Cl-2], the mononuclear complexes show a propensity for the incorporation of water into their crystal lattices; in the case of [Cu(H1)Cl-2]Cl center dot 4H(2)O and [Cu(H1)Cl-2]Cl center dot 4.75H(2)O, the small change in water content leads to the assembly of (5.8(2))(2)(5.6.8)(4)(5(2).6)(2) or (4(2).6(2))(3)(4.6(2))(6) water-chloride ion nets

    The global food chain

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    Jonathon Porritt is Founder Director of Forum for the Future www.forumforthefuture.org.uk; Chairman of the UK Sustainable Development Commission www.sd-commission.org.uk; and author of Capitalism as if the World Matters (Earthscan, 2007)

    Reversibly Tuning the Viscosity of Peptide-Based Solutions Using Visible Light

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    Light can be used to design stimuli–responsive systems. We induce transient changes in the assembly of a low molecular weight gelator solution using a merocyanine photoacid. Through our approach, reversible viscosity changes can be achieved via irradiation, delivering systems where flow can be controlled non-invasively on demand.</p

    A Bridge Too Far: Testing the Limits of Polypyridyl Ligands in Bridging Soluble Subunits of a Coordination Polymer

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    Starting with a coordination polymer, {[Cu(L)]2}n (1 where H2L = salicylidene-2-aminophenol), we have explored the ability of polypyridyl ligands (P) to bridge the monomer complex to form nine {[Cu(L)]2(P)} complexes. The identity and solution stability of the [Cu(L)] units has been investigated through a novel combined UV–vis/EPR experiment and it has been found to be a stable supramolecular building unit for the construction of discrete complexes and coordination polymers. The reorganization of [Cu(L)] units to a new coordination polymer on addition of 4,4′-bipyridine markedly changes the connectivity of the structure and the magnitude of the antiferromagnetic interactions through reorientation of the Cu(II) orbitals. We also present the structure of 1, 80 years after its synthesis was first reported

    A conceptual review of interprofessional expertise in child safeguarding

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    It is increasingly accepted that practitioners across a range of professional fields must work together in order to promote children's welfare and protect them from harm. However, it has also become apparent that interprofessional working is a challenging area of practice that cannot simply be prescribed through protocols and procedures, nor acquired as a set of technical competences. This article develops the concept of interprofessional expertise in order to explain how practitioners become more proficient at working with others to manage complex child welfare issues. Key principles are outlined with reference to relevant theoretical frameworks, including models of skill acquisition. The article concludes by discussing some potential implications for future research and contemporary developments in child safeguarding practice

    Metal Template Synthesis of Molecular Knots and Links

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    The use of metal ions as templates to direct the assembly of complex architectures and topologies is briefly reviewed, highlighting milestones in the field from [2]catenanes, through to trefoil knots, Solomon links, Borromean rings and most recently to a molecular pentafoil knot

    Crystal engineering with 2,2':6',2"- terpyridine derivatives and their metal complexes : from simple building blocks to coordination polymers and networks

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    This thesis concerns the design of ligands for use in the construction of larger supramolecular systems, with emphasis on the application of 4'-substitured 2,2',6',2''- terpyridine ligands and their iron(II) and ruthenium(II) complexes in crystal engineering. The first section considers 4'-hydrazone functionalized 2,2',6',2''-terpyridines and their dynamic behaviour in solution and structural characteristics in the solid state, with respect to protonation. Neutral, mono- and di-protonated ligands are considered. The iron(II) and ruthenium(II) complexes of these ligands are reported and their properties studied by variable temperature NMR, UV-visible spectroscopy and single crystal X-ray crystallography. Subtle changes in substituents were found to have dramatic effects on crystal packing and some common packing arrangements were identified. A range of potential ‘expanded ligands’ (complexes which can themselves act as ligands for additional metal centres), are introduced in the next section. These can be potentially used to bridge metal centres to form both discrete and infinite structures, in particular in the solid state. In a systematic study of single crystal X-ray crystal structures of these complexes many were found to be more flexible than they first appear, and that the crystal packing arrangements were often sensitive to solvent. The next section describes the first crystallographically characterized coordination polymers and networks which include metal bis(terpyridine) units. Self-complementary hydrogen bonding was also found to be a stabilizing motif, with a number of such structures prepared. The final chapter blends the ideas of previous sections: 4'-(x-pyridyl) functionalized 2,2',6',2''-terpyridine ligands are used to form ‘expanded ligands’ with iron(II) and ruthenium(II) centres. These were characterized in solution, with protonation of the distant pendant pyridyl ring found to significantly influence the MLCT absorption of the complexes. These complexes were incorporated into two larger structures and characterised by single crystal X-ray crystallography. A selfcomplementary hydrogen bonded polymer which possesses nanopores through the crystal lattice is reported. Iron bis(thiocyanate) was also used to form a bridged coordination polymer
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