{"product_id":"organic-crystal-engineering-isbn-9780470319901","title":"Organic Crystal Engineering","description":"\u003ci\u003eOrganic Crystal Engineering\u003c\/i\u003e provides reviews of topics in organic crystal engineering that will be of interest to all researchers in molecular solid-state chemistry. Specialist reviews written by internationally recognized researchers, drawn from both academia and industry, cover topics including crystal structure prediction features, polymorphism, reactions in the solid-state, designing new arrays and delineating prominent intermolecular forces for important organic molecules.  List of Contributors.  \u003cp\u003ePreface.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1 The Role of the Cambridge Structural Database in Crystal Engineering (\u003c\/b\u003e\u003ci\u003eAndrew D. Bond\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e1.1 Introduction.\u003c\/p\u003e \u003cp\u003e1.2 Organisation and Management of Crystallographic Information.\u003c\/p\u003e \u003cp\u003e1.3 Organisation of Crystallographic Information for Crystal Engineering.\u003c\/p\u003e \u003cp\u003e1.4 New Tools for Database Research.\u003c\/p\u003e \u003cp\u003e1.5 Search for Functional Group Exchanges: GRX.\u003c\/p\u003e \u003cp\u003e1.6 Search for Solvated and Unsolvated Structures: Solvates.\u003c\/p\u003e \u003cp\u003e1.7 Clustering and Classifying CSD Search Results: dSNAP.\u003c\/p\u003e \u003cp\u003e1.8 The PXRD Profile as a Structural Descriptor.\u003c\/p\u003e \u003cp\u003e1.9 Identifying Supramolecular Constructs: XPac.\u003c\/p\u003e \u003cp\u003e1.10 Concluding Remarks: the Future Role of Crystallographic Databases.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2 Computational Crystal Structure Prediction: Towards \u003ci\u003eIn Silico\u003c\/i\u003e Solid Form Screening (\u003c\/b\u003e\u003ci\u003eGraeme M. Day\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e2.1 Introduction.\u003c\/p\u003e \u003cp\u003e2.2 Methods used to Predict Crystal Structures.\u003c\/p\u003e \u003cp\u003e2.3 Current Capabilities of Crystal Structure Prediction.\u003c\/p\u003e \u003cp\u003e2.4 Exploration of Crystal Forms. A Case Study: Carbamazepine.\u003c\/p\u003e \u003cp\u003e2.5 Summary.\u003c\/p\u003e \u003cp\u003eAcknowledgments.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3 Multi-component Pharmaceutical Crystalline Phases: Engineering for Performance (\u003c\/b\u003e\u003ci\u003eMatthew L. Peterson, Edwin A. Collier, Magali B. Hickey, Hector Guzman and Örn Almarsson\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e3.1 Introduction.\u003c\/p\u003e \u003cp\u003e3.2 Exploring Crystal Form Diversity.\u003c\/p\u003e \u003cp\u003e3.3 High-throughput Experimentation.\u003c\/p\u003e \u003cp\u003e3.4 Examples of ‘Form and Formulation’.\u003c\/p\u003e \u003cp\u003e3.5 AMG517 and Celecoxib – ‘Spring and Parachute’ Approach.\u003c\/p\u003e \u003cp\u003e3.6 Carbamazepine - Stabilization Against a Hydrate.\u003c\/p\u003e \u003cp\u003e3.7 Theophylline:Phenobarbital - Two is Better Than One.\u003c\/p\u003e \u003cp\u003e3.8 Delaviridine Mesylate - Material Misbehavior.\u003c\/p\u003e \u003cp\u003e3.9 Summary and Outlook.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4 Complex Formation of Surfactants with Aromatic Compounds and their Pharmaceutical Applications (\u003c\/b\u003e\u003ci\u003eYuji Ohashi, Keiju Sawada and Nahoko Iimura\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e4.1 Introduction.\u003c\/p\u003e \u003cp\u003e4.2 Structures of the Complexes Formed Between Surfactants and Aromatic Compounds.\u003c\/p\u003e \u003cp\u003e4.3 Complex Formation of Aromatic Compounds Containing an Hetero Ring.\u003c\/p\u003e \u003cp\u003e4.4 Complex Formation of Biphenyl with Cationic Surfactants.\u003c\/p\u003e \u003cp\u003e4.5 Complex Formation of Odd-Number Surfactants with Biphenyl.\u003c\/p\u003e \u003cp\u003e4.6 Common Packing Mode in the Complexes.\u003c\/p\u003e \u003cp\u003e4.7 Complex Formation by Grinding in a Mortar.\u003c\/p\u003e \u003cp\u003e4.8 C-H...\u003ci\u003ep\u003c\/i\u003e interactions.\u003c\/p\u003e \u003cp\u003e4.9 Complex Formation of Anionic Surfactants with Aromatic Compounds.\u003c\/p\u003e \u003cp\u003e4.10 Increased Solubility of Insoluble Drugs.\u003c\/p\u003e \u003cp\u003e4.11 Enhanced Thermal Stability of Perfumes.\u003c\/p\u003e \u003cp\u003e4.12 Complex Formation with Surfactants other than Quaternary Alkylammonium Salts.\u003c\/p\u003e \u003cp\u003e4.13 Hydroquinone Complexes.\u003c\/p\u003e \u003cp\u003e4.14 Application to Whitening Agents.\u003c\/p\u003e \u003cp\u003eAcknowledgments.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5 Hydrogen Bonding and Molecular Packing in Multi-Functional Crystal Structures (\u003c\/b\u003e\u003ci\u003eAshwini Nangia\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e5.1 Introduction.\u003c\/p\u003e \u003cp\u003e5.2 Hydrogen Bonding in Ureas and Amides.\u003c\/p\u003e \u003cp\u003e5.3 Pyridyl Ureas and Amides.\u003c\/p\u003e \u003cp\u003e5.4 Nitrophenyl Ureas and Amides.\u003c\/p\u003e \u003cp\u003e5.5 Molecular Conformation and Hydrogen Bonding.\u003c\/p\u003e \u003cp\u003e5.6 Supramolecular HSAB Interactions.\u003c\/p\u003e \u003cp\u003e5.7 \u003ci\u003egem\u003c\/i\u003e-alkynols.\u003c\/p\u003e \u003cp\u003e5.8 Conclusions.\u003c\/p\u003e \u003cp\u003eAcknowledgments.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6 Persistence of N-H...S Hydrogen Bonding in Thiocarbamide Structures (\u003c\/b\u003e\u003ci\u003eEdward R. T. Tiekink\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e6.1 Introduction.\u003c\/p\u003e \u003cp\u003e6.2 Supramolecular Aggregation Patterns in the Thiocarbamides.\u003c\/p\u003e \u003cp\u003e6.3 Conclusions.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7 Crystal Engineering with the Molecules Containing Amide and Pyridine Functionalities (\u003c\/b\u003e\u003ci\u003eKumar Biradha and Lalit Rajput\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e7.1 Introduction.\u003c\/p\u003e \u003cp\u003e7.2 Primary Amides Containing the Pyridine Moiety.\u003c\/p\u003e \u003cp\u003e7.3 Co-crystals with Primary Amidopyridines.\u003c\/p\u003e \u003cp\u003e7.4 Secondary Amides Containing a Pyridine Moiety.\u003c\/p\u003e \u003cp\u003e7.5 Bis-Amidopyridine Derivatives.\u003c\/p\u003e \u003cp\u003e7.6 Two-component Structures Containing Secondary Amides and Pyridine Derivatives.\u003c\/p\u003e \u003cp\u003e7.7 Triamidopyridine Derivatives.\u003c\/p\u003e \u003cp\u003e7.8 Conclusions.\u003c\/p\u003e \u003cp\u003eAcknowledgements.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8 Urea\/Thiourea-Anion Host Lattices, Stabilization of Labile Species, and Designed Construction of Rosette Ribbon and Layers (\u003c\/b\u003e\u003ci\u003eThomas C. W. Mak, Chi-Keung Lam, Jie Han, Qi Li and Feng Xue\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e8.1 Introduction.\u003c\/p\u003e \u003cp\u003e8.2 Inclusion Compounds with Urea\/Thiourea-Anion Host Lattices.\u003c\/p\u003e \u003cp\u003e8.3 Stabilization of Cyclic Oxocarbon Dianions by Hydrogen Bonding with Urea\/Thiourea.\u003c\/p\u003e \u003cp\u003e8.4 Supramolecular Assembly Based on the Rosette Motif.\u003c\/p\u003e \u003cp\u003e8.5 Conclusion and Outlook.\u003c\/p\u003e \u003cp\u003eAcknowledgments.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eIndex.\u003c\/p\u003e  \u003cp\u003eEdward R. T. Tiekink is the editor of Organic Crystal Engineering: Frontiers in Crystal Engineering, published by Wiley. Jagadese Vittal is the editor of Organic Crystal Engineering: Frontiers in Crystal Engineering, published by Wiley.   Crystal Engineers are dedicated to controlling the way molecules aggregate in the crystalline phase and therefore are concerned with crystal structure prediction, polymorphism, and discovering the relative importance of different types of intermolecular forces and their influence on molecular structure. Crystal Engineers are exploiting the fruits of their labours by discovering new and important properties of their new materials.  \u003c\/p\u003e\u003cp\u003e\u003ci\u003eOrganic Crystal Engineering\u003c\/i\u003e provides reviews of topics in this field that will be of interest to all researchers in molecular solid-state chemistry. Specialist reviews written by internationally recognized researchers, drawn from both academia and industry, include discussions on:\u003c\/p\u003e \u003cul type=\"disc\"\u003e \u003cli\u003ethe role of the Cambridge Structural Database in crystal engineering\u003c\/li\u003e \u003cli\u003ecomputational crystal structure prediction: towards \u003ci\u003ein silico\u003c\/i\u003e solid form screening\u003c\/li\u003e \u003cli\u003emulti-component pharmaceutical crystalline phases: engineering for performance\u003c\/li\u003e \u003cli\u003ecomplex formation of surfactants with aromatic compounds and their pharmaceutical applications\u003c\/li\u003e \u003cli\u003ehydrogen bonding and molecular packing in multi-functional crystal structures\u003c\/li\u003e \u003cli\u003epersistence of N–H...S hydrogen bonding in thiocarbamide structures\u003c\/li\u003e \u003cli\u003ecrystal engineering with the molecules containing amide and pyridine functionalities\u003c\/li\u003e \u003cli\u003eurea\/thiourea-anion host lattices, stabilization of labile species, and designed construction of rosette ribbon and layers\u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003e\u003ci\u003eOrganic Crystal Engineering\u003c\/i\u003e follows on from the successful \u003ci\u003eFrontiers in Crystal Engineering\u003c\/i\u003e (Wiley, 2005), providing 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","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47989727690981,"sku":"NP9780470319901","price":258.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9780470319901.jpg?v=1761785268","url":"https:\/\/k12savings.com\/es\/products\/organic-crystal-engineering-isbn-9780470319901","provider":"K12savings","version":"1.0","type":"link"}