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Â¡ÖØÍÆ¼öÒ»¸ö£¬ÆäËûµÄÕûÀíÕûÀíÔÙÍÆ¼ö¡£ Research Perspectives during 40 Years of the Journal of Catalysis Frank S. Stone Journal of Catalysis Volume 216, Issues 1-2, May-June 2003, Pages 2-11 Abstract Research developments recorded in the Journal of Catalysis over the past 40 years are reviewed. The journal was launched at a propitious time, as is made clear from the accounts presented of various topics newly introduced in the 1960s, which laid the foundation for achievements to come later, notably in catalysis by zeolites but also in reactions catalyzed by metals and transition metal oxides. The early years are shown to have been followed by a period marked by the skilled application of new experimental techniques, especially spectroscopic methods for catalyst characterization and chemisorption. Research in which ideas and methodology were interchanged between homogeneous and heterogeneous catalysis are also indicated. By the middle years perspectives in catalysis were becoming strongly influenced by concerns regarding oil reserves and care of the environment. Examples of fundamental research reflecting this are described. The article briefly digresses to recall the members who have composed the editorial team of the Journal of Catalysis over the past 40 years, all of them personally active in basic research and recognizable from their work as sympathetic to the drive for understanding catalysis at the molecular level. In a final section the survey returns to its leitmotiv when some research themes from recent years are collated, among them the continuing progress with zeolite-related catalysis, the search for improved enantioselective catalysts, and the application of techniques in theoretical chemistry to chart catalytic reaction mechanisms. ÉϰñÀíÓÉ£º ºÇºÇ£¬ÕâÀà×ÛÊö²»¶à¼û°É¡£Journal of catalysisÊÇ×îºÃµÄ´ß»¯ÀàÑо¿ÂÛÎÄÆÚ¿¯£¬×÷ÕßÊÇ´ß»¯ÔÓÖ¾µÄÖ÷±à£¬»Ø¹ËÁËJ.CËÄÊ®ÄêÀ´¶Ô´ß»¯½çµÄ¹±Ïס£¼òÖ±¾ÍÏ൱ÓÚ60ÄêÖ®ºóµÄ´ß»¯¼òÊ·£¬ºÇºÇ£¡¸ß¶È£¬Ñ۽綼ÊÇûµÃ˵µÄ¡£ ÎÞÂÛ¶ÔÓÚÈëÃż¶ÐÂÊÖÀ´Ëµ£¬»¹ÊÇ´ß»¯ÀÏÄñ£¬¶¼ÖµµÃ×Ðϸȥ¶Á¡£ ¶Áºó£¬Äã»á·¢ÏÖ£¬60Äê´úºó´ß»¯·¢Õ¹µÄÀï³Ì±®Ê½µÄ¶«Î÷£¬¼¸ºõ¶¼ÔÚÀïÃæ¡£¶øÇÒÆäÒýÓõIJο¼ÎÄÏ×£¬´ó¶àÊǾµäÖ®Öеľµä¡£À©Õ¹ÆðÀ´Ê¤¹ýÒ»±¾½Ì¿ÆÊé¡£ ±È½ÏרҵµÄÎÄÏ×£¬ÎҵûØÈ¥ÏêϸÕûÀíÕûÀí²ÅÄÜÄóöÀ´¡£ºÇºÇ¡£¹À¼Æ±È½Ï·Ñʱ¼ä¡£¿ÉÄܰë;¶ø·Ï¡£ºÇºÇ¡£ [ Last edited by smallfolk on 2007-11-20 at 15:49 ] |
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ÎÒ¾õµÃÕâ¸ö£º Heterogeneous Basic Catalysis Hideshi Hattori Chem. Rev. 1995, 95. 537-550 ÎÒÖ÷Òª×÷¹ÌÌå¼îÓ¦ÓúÍCH4ÖØÕû·½Ã棬ÒÔÏÂÊÇÕâ·½ÃæÎÒÈÏΪ±È½ÏÅ£µÄ¼¸Æª CO2 Reforming of CH4 M. C. J. BRADFORD* and M. A. VANNICE CATAL. REV.¡ªSCI. ENG., 41(1), 1¨C42 (1999) BINARY MgO-BASED SOLID SOLUTION CATALYSTS FOR METHANE CONVERSION TO SYNGAS Yun Hang Hu*,† and Eli Ruckenstein CATALYSIS REVIEWS, 44(3), 423¨C453 (2002) ¹ØÓÚ¼×Í鲿·ÖÑõ»¯µÄ£º Brief overview of the partial oxidation of methane to synthesis gas Andrew P.E. York, Tiancun Xiao, and Malcolm L.H. Green Topics in Catalysis Vol. 22, Nos. 3¨C4 345 [ Last edited by ratio on 2007-11-22 at 23:23 ] |
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Hoffmann, M. R. Martin, S. T. Choi, W. Y. Bahnemann, D. W Environmental Applications of Semiconductor Photocatalysis Chem. Rev. 1995, 95, 69-96 Contents I. Introduction A. General Background B. Semiconductor Photocatalysis II. Mechanisms of Semiconductor Photocatalysis A. Basic Features and Characteristic Times B. Formation of Reactive Oxygen Species III. Chemical Kinetics of Semiconductor Photocatalysis A. Heterogeneous Photochemical Kinetics 1. Reaction Stoichiometry 2. Reaction Rates, Surface Interactions, and Quantum Efficiencies B. Surface Chemistry of Metal Oxide Semiconductors C. Langmuir-Hinshelwood Kinetics D. Heterogeneous Quantum Efficiencies E. Sorption of Electron Donors and Acceptors IV. Bulk-Phase Semiconductors A. Metal Oxide Semiconductors and TiOn B. Metal Ion Dopants and Bulk-Phase Photoreactivity V. Quantum-Sized Semiconductors A. Basic Characteristics and Behavior B. Doped Quantum-Sized TiOn VI. Photochemical Reactors A. Water Treatment Systems B. Gas-Phase Treatment Systems VII. Important Reaction Variables VIII. Photochemical Transformation of Specific Compounds A. Inorganic Compounds B. Organic Compounds IX. Mechanistic Aspects of Selected Reactions A. Chloroform B. Pentachlorophenol C. Glyoxylic Acid D. Acetic Acid E. Carbon Tetrachloride F. 4-Chlorophenol X. Conclusions XI. Acknowledgments XII. References ÕâÆª×ÛÊö´Ó°ëµ¼Ìå¹â´ß»¯µÄ±³¾°×ÅÊÖ£¬²ûÊöÁ˰뵼Ìå´ß»¯µÄ»úÖÆÓëÆä»¯Ñ§¶¯Á¦Ñ§¹ØÏµ£¬±È½ÏÁ˾ßÌå²ÄÁϵĿé²ÄºÍÄÉÃ׳߶ÈϵIJî±ð£¬ÌÖÂÛÁ˲»Í¬¹â´ß»¯ÌåϵÒÔ¼°¹â´ß»¯¹ý³ÌÖеÄÖØÒª±äÁ¿ÒÔ¼°Ò»Ð©²»Í¬»¯Ñ§»ùÍŵķ´Ó¦¡£ |
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¡¾×÷Õß¡¿Peter I. Dalko and Lionel Moisan, ¡¾ÎÄÌâ¡¿Enantioselective Organocatalysis ¡¾ÆÚ¿¯Ãû£¬Äê·Ý£¬¾í£¨ÆÚ£©£¬ÆðÖ¹Ò³Âë¡¿Angew. Chem. Int. Ed. 2001, 40, 3726-3748 ¡¾¡¾×÷Õß¡¿Peter I. Dalko and Lionel Moisan, ¡¾ÎÄÌâ¡¿In the Golden Age of Organocatalysis ÆÚ¿¯Ãû£¬Äê·Ý£¬¾í£¨ÆÚ£©£¬ÆðÖ¹Ò³Âë¡¿Angew. Chem. Int. Ed. 2004, 43, 5138-5175. ÍÆ¼öΪ¾µäµÄÀíÓÉ£ºÓлúС·Ö×Ó´ß»¯×îȨÍþµÄÁ½Æª×ÛÊö |
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ÌṩÁ½ÆªJACSµÄÎÄÕ£¬Ò»ÆªÊÇÓлú¹è¾ùÏà´ß»¯·½ÃæµÄ¾µä¡£ J. L. Speier, J. A. Webster, C. H. Barnes, J. Am. Chem. Soc. 79(1957)974. ÁíһƪҲÊÇJACSµÄÎÄÕ£¬½«Àë×ÓÒºÌåºÍÓлú¹è¹èÇâ¼Ó³É·½ÃæµÄ¾«Æ·¡£ T. J. Geldbach, D. B. Zhao, N. C. Castillo, G. Laurenczy, B. Weyershausen, P. J. Dyson, J. Am.Chem. Soc. 128(2006)9773. |
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ÎÒÊÇ×öÎ²ÆøÖеªÑõ»¯Îï´ß»¯·Ö½â¿ÎÌ⣬ÎÒ¶ÁÕâ·½ÃæµÄÎÄÏ×¾õµÃ½ÏºÃµÄ×ÛÊöÐÔÎÄÕÂÓм¸Æª£º ¡¾1¡¿.Freek Kapteijn * , Jo& Rodriguez-Mirasol , Jacob A. Moulijn Heterogeneous catalytic decomposition of nitrous oxide Applied Catalysis B: Environmental 9 (1996) 25-64 ¡¾2¡¿.J. P¨¦rez-Ram´ırez , F. Kapteijn , K. Schöffel , J.A. Moulijn Formation and control of N2O in nitric acid production Where do we stand today? Applied Catalysis B: Environmental 44 (2003) 117¨C151 ¡¾3¡¿.William C. Trogler Physical properties and mechanisms of formation of nitrous oxide Coordination Chemistry Reviews 187 (1999) 303-327 ¡¾4¡¿.F. Garin. Mechanism of NOx decomposition[J]. Applied Catalysis A:General, 2001(222):183¨C219. ÓÈÆäÊÇÎÄÏ×2ºÍ4£¬¶¼±È½ÏУ¬Ð´µÃºÃÏêϸµÄ¡£ [ Last edited by aiyuanzh on 2007-11-23 at 17:18 ] |
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ÊÖÍ·ÓÐÁ½Æª¸ú´ß»¯Å¼ÁªÓйصÄrev 1.Chem. Rev. 1995, 95,2457-2483 2451 Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds Norio Miyaura' and Akira Suzuki'nt ÕâÆªµÄ×÷ÕßÊÇSuzuki-Miyaura·´Ó¦µÄ¿ªÉ½±ÇÖ÷°¡£¬ÏàÐÅÓ¦¸ÃÎÞÈ˲»Öª°É£¡ 2.Chem. Rev. 2006, 106, 2651-2710 Selected Patented Cross-Coupling Reaction Technologies Jean-Pierre Corbet and Ge´rard Mignani* ¸öÈ˾õµÃÕâ¸öÎÄÕ¶ÔÓÚÏëÒªÈëÃźÜÊʺϣ¬ÓÐÏ꾡µÄ¸÷ÖÖ´ß»¯Å¼ÁªµÄ·´Ó¦µÄ½éÉܺÍÇ°ÑØÇé¿ö£¬¶øÇÒ½éÉÜÁËËûÃǵĹ¤ÒµºÏ³ÉµÄ¿ÉÄܺͼÛÖµ£¡ |
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¶¥¿´µ½Í¬ÐÐÁË£¬Pd´ß»¯µÄÕâ±ßÒ²²»ÉÙ°¡ Ìû¼¸ÆªsanfordµÄ 1.Reactivity of Pd(II) Complexes with Electrophilic Chlorinating Reagents: Isolation of Pd(IV) Products and Observation of C-Cl Bond-Forming Reductive Elimination Published on Web 11/16/2007 jacs 2.Synthesis of Cyclopropanes via Pd(II/IV)-Catalyzed Reactions of Enynes Published on Web 04/14/2007 jacs 3.Catalytic and Highly Regioselective Cross-Coupling of Aromatic C-H Substrates Published on Web 09/11/2007 jacs sanford epartment of Chemistry, UniVersity of MichiganËûÃÇС×é×öµÄ¿ÎÌâ×ܸøÈ˺ÜǰհµÄ¸Ð¾õ£¬ÉÏÃæÊÇÎÒ¿´¹ýµÄ07ÄêµÄ¼¸Æªjacs¡£·ÖÏíÏ£¡ |
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Title: Industrial biocatalysis today and tomorrow Author(s): Schmid A, Dordick JS, Hauer B, Kiener A, Wubbolts M, Witholt B Source: NATURE 409 (6817): 258-268 JAN 11 2001 Document Type: Review Language: English Cited References: 101 Times Cited: 426 Abstract: The use of biocatalysis for industrial synthetic chemistry is on the verge of significant growth. Biocatalytic processes can now be carried out in organic solvents as well as aqueous environments, so that apolar organic compounds as well as water-soluble compounds can be modified selectively and efficiently with enzymes and biocatalytically active cells. As the use of biocatalysis for industrial chemical synthesis becomes easier, several chemical companies have begun to increase significantly the number and sophistication of the biocatalytic processes used in their synthesis operations. link:http://www.nature.com/nature/journal/v409/n6817/abs/409258a0.html;jsessionid=9BF4167444A25681CA78DFB53A527344 Ç¿ÁÒÍÆ¼ö´ÓÊÂÉúÎï´ß»¯µÄccÔĶÁ´ËÎÄ£¬ÕâÊǸÃÁìÓòµÄ¾µä´ó×÷Ö®Ò»£¬´ÓijÖÖÒâÒåÉÏÀ´ËµÒѾÒѳÉΪÉúÎï´ß»¯×¨Òµ±Ø¶ÁÎÄÏ×£¬´Ó2001µ½2007½ö½ö6Äê¼ä¾Í±»ÒýÓÃ426´Î£¬ÓÖÊÇ·¢±íÔÚ¹ú¼Ê¶¥¼âÔÓÖ¾nature£¬·ÖÁ¿¿É¼ûÒ»°ß¡£ [ Last edited by hqsinberg on 2007-11-24 at 01:49 ] |
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¡¾×÷Õß¡¿A. Coma ¡¾ÎÄÌâ¡¿Inorganic Solid Acids and Their Use in Acid-Catalyzed Hydrocarbon Reactions ¡¾ÆÚ¿¯Ãû£¬Äê·Ý£¬¾í£¨ÆÚ£©£¬ÆðÖ¹Ò³Âë¡¿Chem. Rev. 1995, 95, 559414 ¡¾È«ÎÄÁ´½Ó»òÊý¾Ý¿âÃû³ÆÕªÒª£¨ÖÐÓ¢Îľù¿É£©£»Contents I. Nature of Acid Sites on Solid Acid Catalysts II. Physicochemical Characterization of Surface Acidity A. Titration Methods B. Adsorption and Temperature-Programmed Desorption of Base Molecules C. Vibrational Spectroscopy Methods D. Nuclear Magnetic Resonance Methods E. Photoelectron Spectroscopy Methods F. Surface Acidity from the Analysis of the Positron Annihilation Line Shapes G. Conclusions 111. Solid Acid Catalysts 568 A. Amorphous Silica-Alumina and Aluminum 568 Phosohate B. Zeoliies and Zeotypes as Solid Acid 570 Catalvsts 1. Zeolites as Microreactors 570 2. Nature of Acid Sites 573 3. Influence of Chemical Composition on 574 Number and Strength of Acid Sites 4. influence of Structural Effects 576 5. Confinement Effects 577 6. Soft-Hard Acidities in Zeolites 577 7. Interaction between Hydrocarbons and 578 Acid Sites: Carbocations as Intermediates in Acid-Catalyzed Reactions on Zeolites 8. Zeolites as Acid Catalysts for Hydrocarbon Reactions C. Heteropoly Acids 1. Composition, Structure Preparation, and Textural Properties 2. Nature of Acid Sites 3. Acid-Catalyzed Hydrocarbon Reactions by Heteropoly Compounds 1. Preparation of Sulfated Metal Oxides 2. Nature of Acid Sites 3. Hydrocarbon Reactions on Superacids D. Sulfated Metal Oxides Oxides and Sulfated Oxides IV. General Conclusions V. References ÍÆ¼öΪ¾µäµÄÀíÓÉ£º½²µ½´ß»¯£¬²»Äܲ»Ìá¹ÌÌåËá¼î°É£¬´Ó¹èÂÁСÇò¡¢¹èÔåÍÁ¡¢·Ðʯ·Ö×Óɸ£¬¹ÌÌåËá´ß»¯¼ÁÒ»Ö±°éËæ×ÅʯÓ͹¤ÒµºÍʯÓÍ»¯Ñ§¡¢¾«Ï¸»¯¹¤µÄ·¢Õ¹£¬CormaÔòÊǹÌÌåËá´ß»¯ÁìÓòÖеĸßÊÖ£¬ËûµÄ¶àƪרÀû¶Ô´ß»¯Ñ§ÕßÀ´½²·Ç³£ÖØÒª£¬ÏÈÕûÀí³öһƪ¡£ |
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ÎÒÍÆ¼ö×îд߻¯·¼»ùÄ©¶ËȲºÏ³É·½ÃæµÄ×ÛÊö£º The Sonogashira Reaction:A Booming Methodology in Synthetic Organic Chemistry. Rafael Chinchilla and Carmen Najera Chem.Rev.2007.107.874-922 Contents 1. Introduction 2. Mechanistic Considerations 3. Catalysts and Reaction Conditions 3.1. Palladium-Phosphorus Complexes 3.1.1. Unsupported Palladium-Phosphorus Complexes 3.1.2. Supported Palladium-Phosphorus Complexes 3.2. Palladium-Nitrogen Complexes 3.2.1. Unsupported Palladium-Nitrogen Complexes 3.2.2. Supported Palladium-Nitrogen Complexes 3.3. Palladium-P,N- and Palladium-P,O Complexes 3.4. N-Heterocyclic Carbene (NHC) Palladium Complexes 3.4.1. Unsupported NHC Palladium Complexes 3.4.2. Supported NHC Palladium Complexes 3.5. Palladacycle Catalysts 3.5.1. Unsupported Palladacycles 3.5.2. Supported Palladacycles 3.6. Ligand-Free Palladium Catalysts 3.6.1. Unsupported Ligand-Free Palladium Catalysts 3.6.2. Solid-Supported Ligand-Free Palladium Catalysts 3.7. Palladium Nanoparticles as Catalysts 3.8. Other Transition-Metal Complexes 3.9. Transition-Metal-Free Reactions 4. Applications 4.1. Alkynylation of Arenes 4.2. Alkynylation of Heterocycles 4.3. Synthesis of Enynes and Enediynes 4.4. Synthesis of Ynones 896 4.5. Synthesis of Carbocyclic Systems 4.6. Synthesis of Heterocyclic Systems 4.7. Synthesis of Natural Products 4.8. Synthesis of Electronic and Electrooptical Molecules 4.9. Synthesis of Molecules for Nanostructures 5. Conclusions 6. Acknowledgments 7. References ¹ØÓÚ·¼»ùÄ©¶ËȲµÄºÏ³É·´Ó¦¼´ÖøÃûµÄSonogahshira·´Ó¦£¬´Ó1975ÄêÌá³öµ½½ñÌìÒѾ¹ýÈ¥Á˽ü30Ä꣬ÔÚ»¯Ñ§Êý¾Ý¿âÀïÃæÊäÈëSonogahshira¹Ø¼ü´Ê¿ÉÒÔ·¢ÏÖ£¬½üÁ½ÄêµÄÑо¿ÂÛÎÄÊýÒѾ³¬¹ýÍíÄêµÄ×ܺͣ¬¿É¼ûÕâ¸ö·´Ó¦ÒѾԽÀ´Ô½¶àµÄÊÕµ½ÈËÃǵÄÖØÊÓ¡£¶øÕâÆª×ÛÊöÊÇĿǰΪֹΨһµÄһƪ×ÛÊö¡£ ÕâÆª×ÛÊö´Ó»úÀíµÄÑо¿¿ªÊ¼ÌÖÂÛ£¬¶Ô´ß»¯¼ÁîÙµÄÑо¿Ö÷Òª´ÓÅäÌåºÍ¸ºÔØÁ½¸ö·½Ãæ½øÐÐ×ÛÊö¸ÅÀ¨£¬×îºóÁоÙÁËÕâ¸ö·´Ó¦µÄʵ¼ÊÓ¦Ó᣿ÉÒÔ˵£¬ÕâÆª×ÛÊö·Ç³£ºÃµÄ¸øÎÒÃǹ´ÀÕ³öSonogashira·´Ó¦µÄȫò£¬ËùÒÔÎÒÇ¿ÁÒÍÆ¼ö×ö¹â²ÄÁϺÍÒ©ÎïÖмäÌåµÄÅóÓÑÃÇ¿´¿´ÕâÆªÎÄÕ¡£ [ Last edited by eBorland on 2007-11-26 at 16:38 ] |
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Jens Weitkamp, Michael Hunger and Ute Rymsa Base catalysis on microporous and mesoporous materials: recent progress and perspectives Microporous and Mesoporous Materials Volume 48, Issues 1-3, 1 November 2001, Pages 255-270 ºÜÓÐÌØµã,×ÛÊöÁË΢½é¿×²ÄÁÏÔÚ¼î´ß»¯ÁìÓòµÄ×îÐÂÓ¦ÓýøÕ¹ |
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£¨1£©Hidenori Yahiro, Masakazu Iwamoto , ¡¶Copper ion-exchanged zeolite catalysts in deNOx reaction¡·. Applied Catalysis A: General 222 (2001) 163¨C181 ¾ÍÊDZ¾ÎÄ×÷ÕßIwamotoÓÚ1986Ê״η¢ÏÖCu-ZSM-5¶ÔNOµÄ¶ÀÌØµÄ´ß»¯·Ö½â»îÐԵģ¬¿ª´´ÁËеÄÑо¿ÁìÓò£¬´Ó´ËÏÆÆðÁ˶ÔCu-ZSM-5Ñо¿µÄÈȳ±£¬¿ÉÒÔ˵ËûÊÇCu-ZSM-5Ö±½Ó´ß»¯·Ö½âNO·½ÃæµÄ´óţȨÍþÁË£¬ÕâÆªÎÄÕÂдµÄºÜºÃ£¬Ç¿ÁÒÍÆ¼ö¿´¿´¡£ ¸Ã×ÛÊö·ÖÈý¸öСרÌ⣺ 1.Catalytic decomposition of NO on Cu-zeolites 2.Selective catalytic reduction of NO with hydrocarbons in the presence of excess oxygen 3.Adsorption and molecular diffusion of NOx in zeolites ÎÒ¿´Á˾õµÃºÜºÃ¶®£¬±Ï¾¹×÷ÕßÑо¿Cu-ZSM-5½ü¶þÊ®Ä꣬д³öÀ´¸ú±ðµÄÏà¹Ø×ÛÊö¾ÍÊDz»Ò»Ñù £¨2£©V.I. PaÃrvulescua,*, P. Grangeb, B. Delmonb¡£ ¡¶Catalytic removal of NO¡· Catalysis Today 46 (1998) 233-316 ÕâÆªÎÄÏ×ÌâĿֻÓÐËĸöµ¥´Ê£¬¿ÉÊÇÕûÕûдÁË84Ò³£¬Ó¦ÓÃÎÄÏ×645ƪ£¬¿É¼ûÆä·ÖÁ¿£¬ÎÒÒ²¿´ÁË£¬¾õµÃ²»´í£¬Ëĸö×ÖÐÎÈÝ£ºÈ«ÃæÏêϸ ÕÒ²»µ½ÔÎĵÄPMÎÒ |
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ÌâÄ¿£ºReduced Transition Metal Colloids: A Novel Family of Reusable Catalysts? ×÷ÕߣºAlain Roucoux, Juergen Schulz, Henri Patin ÎÄÏ×£ºChem. Rev., 2002, 102 (10): 3757-3778 ÍÆ¼öÀíÓÉ£ºÕâÆª×ÛÊöÔÚÄÉÃ×´ß»¯¼ÁÖÆ±¸±íÕ÷¼°Ó¦Ó÷½Ãæ¿°³Æ¾µäÁË [ Last edited by mingziyang on 2007-12-22 at 09:14 ] |
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