{"product_id":"frontiers-in-crystal-engineering-hardback-9780470022580","title":"Frontiers in Crystal Engineering (Hardback) 9780470022580","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eFrontiers in Crystal Engineering\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eEdward R. T. Tiekink (Edited by), E Tiekink (Author), Jagadese Vittal (Edited by)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470022580, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 9 December 2005\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e352 pages\u003cbr\u003e25.2 x 17.3 x 2.5 cm, 0.794 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cem\u003e\u003cfont size=\"3\"\u003e\"Both entrenched and budding members of the discipline will find benefit from reading this text.\" (\u003ci\u003eMolecular Crystals \u0026amp; Liquid Crystals\u003c\/i\u003e, Volume 461, 2006)  \u003cp\u003e\"…a useful review of the breadth of activity and leading thinking in the field of crystal design.\" (\u003ci\u003eJournal of the American Chemical Society\u003c\/i\u003e, June 14, 2006)\u003c\/p\u003e\u003c\/font\u003e\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eFRONTIERS IN\u003cb\u003e CRYSTAL ENGINEERING\u003c\/b\u003e  \u003cp\u003eCrystal engineering – where the myriad of intermolecular forces operating in the solid-state are employed to design new nano- and functional materials – is a key new technology with implications for catalysis, pharmaceuticals, synthesis and materials science. \u003c\/p\u003e\n\u003cp\u003e\u003ci\u003eFrontiers in Crystal Engineering \u003c\/i\u003egathers personal perspectives, from inter­national specialists working in molecular aspects of crystal engineering, on the practical and theoretical challenges of the discipline, and future prospects. These demonstrate the approaches that are being used to tackle the problems associated with the complexity, design and functionality of crytalline molecular solids. \u003c\/p\u003e\n\u003cp\u003eTopics include \u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ehow intermolecular forces direct and sustain crystal structures\u003c\/li\u003e \u003cli\u003efunctional engineering and design elements\u003c\/li\u003e \u003cli\u003ecoordination polymers and network structures\u003c\/li\u003e \u003cli\u003eapplications in green and pharmaceutical chemistry\u003c\/li\u003e\n\u003c\/ul\u003e \u003cp\u003e\u003ci\u003eFrontiers in Crystal Engineering\u003c\/i\u003e is a useful guide to this exciting new discipline for both entrants to the field as well as established practitioners, and for those working in crystallography, medicinal and pharmaceutical sciences, solid-state chemistry, and materials and nanotechnology.\u003c\/p\u003e\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cb\u003eList of Contributors.\u003c\/b\u003e  \u003cp\u003e\u003cb\u003eForeword.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1. Applications of Crystal Engineering Strategies in Solvent-free Reactions: Toward a Supramolecular Green Chemistry.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e1 Mechanochemical preparation of Hydrogen-Bonded Adducts.\u003c\/p\u003e \u003cp\u003e1 Mechanically induced formation of covalent bonds.\u003c\/p\u003e \u003cp\u003e1 The solvent-free chemistry of the zwitterion.\u003c\/p\u003e \u003cp\u003e1 Concluding remarks.\u003c\/p\u003e \u003cp\u003e1 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2. Crystal Engineering of Pharmaceutical Co-crystals.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 What is the origin of polymorphism and is it prevalent in co-crystals?.\u003c\/p\u003e \u003cp\u003e3 What is the pharmaceutical co-crystal?.\u003c\/p\u003e \u003cp\u003e4 Conclusions.\u003c\/p\u003e \u003cp\u003e5 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3. Template-controlled Solid-state Synthesis: Toward a General Form of Covalent Capture in Molecular Solids.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Controlling reactivity using linear templates.\u003c\/p\u003e \u003cp\u003e3 Template-controlled solid-state reactivity.\u003c\/p\u003e \u003cp\u003e4 Target-oriented organic synthesis in the organic state.\u003c\/p\u003e \u003cp\u003e5 Other linear templates.\u003c\/p\u003e \u003cp\u003e6 Summary and outlook.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4. Interplay of Non-covalent Bonds: Effect of Crystal Structure on Molecular Structure.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Second-sphere coordination.\u003c\/p\u003e \u003cp\u003e3 Soft coordination environments.\u003c\/p\u003e \u003cp\u003e4 Speciation.\u003c\/p\u003e \u003cp\u003e5 Molecular conformation.\u003c\/p\u003e \u003cp\u003e6 Conclusions.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5. Crystal Engineering of Halogenated Heteroaromatic Clathrate Systems.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Aromatic edge-edge C-H...N dimers.\u003c\/p\u003e \u003cp\u003e3 Heteroatom-1,3-peri interactions.\u003c\/p\u003e \u003cp\u003e4 Molecular pen structures.\u003c\/p\u003e \u003cp\u003e5 Halogenated edge-edge interactions.\u003c\/p\u003e \u003cp\u003e6 Pi-halogen dimer (PHD) interactions.\u003c\/p\u003e \u003cp\u003e7 Molecular bricks, spheres and grids.\u003c\/p\u003e \u003cp\u003e8 Conclusions.\u003c\/p\u003e \u003cp\u003e9 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6. Steric Control over Supramolecular Aggregation: A Design Element in Crystal Engineering?\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Diorganotin carboxylates.\u003c\/p\u003e \u003cp\u003e3 Triorganotin carboxylates.\u003c\/p\u003e \u003cp\u003e4 Binary zinc xanthates.\u003c\/p\u003e \u003cp\u003e5 Bipyridine adducts of zinc dithiophosphates.\u003c\/p\u003e \u003cp\u003e6 Binary mercury dithiocarbamates.\u003c\/p\u003e \u003cp\u003e7 Binary bismuth xanthates.\u003c\/p\u003e \u003cp\u003e8 Conclusions and Outlook.\u003c\/p\u003e \u003cp\u003e9 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7. Incorporating Molecular Hosts into Network Structures.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Hydrogen-bonded structures with CTV.\u003c\/p\u003e \u003cp\u003e3 Coordination polymers.\u003c\/p\u003e \u003cp\u003e4 Extended-arm CTV derivatives and their coordination polymers.\u003c\/p\u003e \u003cp\u003e5 Conclusions.\u003c\/p\u003e \u003cp\u003e6 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8. Interpenetrating Networks.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Notation.\u003c\/p\u003e \u003cp\u003e3 1-D nets.\u003c\/p\u003e \u003cp\u003e4 2-D nets.\u003c\/p\u003e \u003cp\u003e5 3-D nets.\u003c\/p\u003e \u003cp\u003e6 Unusual interpenetration.\u003c\/p\u003e \u003cp\u003e7 Consequences of interpenetration.\u003c\/p\u003e \u003cp\u003e8 Self-penetration.\u003c\/p\u003e \u003cp\u003e9 Entangled but not interpenetrating.\u003c\/p\u003e \u003cp\u003e10 Conclusions.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9. Architecture and Functional Engineering Based on Paddlewheel Dinuclear Tetracarboxylate Building Blocks.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Synthetic strategy.\u003c\/p\u003e \u003cp\u003e3 Architecture engineering based on preorganized building blocks.\u003c\/p\u003e \u003cp\u003e4 Conductive and magnetic properties based on preorganized building blocks.\u003c\/p\u003e \u003cp\u003e5 Porous properties based on preorganized and in situ building blocks.\u003c\/p\u003e \u003cp\u003e6 Conclusion and outlook.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10. Supramolecular Interactions in Directing and Sustaining Coordination Molecular Architectures.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Molecular architectures assembled by hydrogen-bonding interactions.\u003c\/p\u003e \u003cp\u003e3 Molecular architectures assembled VIA ... Interactions.\u003c\/p\u003e \u003cp\u003e4 Metallophilic interactions.\u003c\/p\u003e \u003cp\u003e5 Concluding remarks and outlooks.\u003c\/p\u003e \u003cp\u003e6 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e11. The Structure-directing Influence of Hydrogen Bonding in Coordination Polymers.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 A novel cadmium cyanide network.\u003c\/p\u003e \u003cp\u003e3 Dihydroxybenzoquinone and Chloranilic acid derivatives of Lanthanides.\u003c\/p\u003e \u003cp\u003e4 A stable zinc saccharate network.\u003c\/p\u003e \u003cp\u003e5 Anionic metal-carbonate networks.\u003c\/p\u003e \u003cp\u003e6 Conclusions.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e12. Hydrogen-bonded Coordination Polymeric Structures.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Introduction.\u003c\/p\u003e \u003cp\u003e2 Solid-state supramolecular transformation of hydrogen-bonded 3-D network to 3-D coordination polymetric network structures by thermal dehydration.\u003c\/p\u003e \u003cp\u003e3 Interconvertible solid-state supramolecular transformation.\u003c\/p\u003e \u003cp\u003e4 Solid-state transformation of a helical coordination polymetric structure to a 3-D coordination network structure by thermal dehydration.\u003c\/p\u003e \u003cp\u003e5 Influence of chiral centers on the helicity of the coordination polymers.\u003c\/p\u003e \u003cp\u003e6 Consequences of C=O... interactions.\u003c\/p\u003e \u003cp\u003e7 Supramolecular isomerism.\u003c\/p\u003e \u003cp\u003e8 Starlike channels and hexagonal diamondoid topology.\u003c\/p\u003e \u003cp\u003e9 Hydrogen-bonded helical water molecules inside a staircase 1-D coordination polymer.\u003c\/p\u003e \u003cp\u003e10 Hydrogen-bonded polyrotaxane-like structure containing cyclic (H2O)4 in [Zn(OAc)2(m-bpe)].2H2O.\u003c\/p\u003e \u003cp\u003e11 Summary.\u003c\/p\u003e \u003cp\u003e12 Acknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIndex.\u003c\/b\u003e\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley","offers":[{"title":"Brand New","offer_id":52256234471704,"sku":"9780470022580","price":166.48,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470022580.jpg?v=1781274501","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/frontiers-in-crystal-engineering-hardback-9780470022580","provider":"Freshly Printed Books","version":"1.0","type":"link"}