LEADER 01964nam 2200577 a 450 001 9910458725103321 005 20210602172520.0 010 $a1-281-39984-1 010 $a1-78034-457-0 010 $a9786611399849 010 $a90-474-1012-2 035 $a(CKB)1000000000402843 035 $a(EBL)3004029 035 $a(SSID)ssj0000138633 035 $a(PQKBManifestationID)11158385 035 $a(PQKBTitleCode)TC0000138633 035 $a(PQKBWorkID)10100972 035 $a(PQKB)10844221 035 $a(MiAaPQ)EBC3004029 035 $a(Au-PeEL)EBL3004029 035 $a(CaPaEBR)ebr10234694 035 $a(CaONFJC)MIL139984 035 $a(OCoLC)923612577 035 $a(EXLCZ)991000000000402843 100 $a20060403d2006 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aDictionary of gnosis & Western esotericism$b[electronic resource] /$fedited by Wouter J. Hanegraaff in collaboration with Antoine Faivre, Roelof van den Broek, Jean-Pierre Brach 210 $aLeiden ;$aBoston $cBrill$dc2006 215 $a1 online resource (1258 p.) 300 $aDescription based upon print version of record. 311 $a90-04-15231-8 320 $aIncludes bibliographical references and indexes. 327 $a""CONTENTS""; ""INTRODUCTION""; ""ACKNOWLEDGMENTS""; ""LIST OF CONTRIBUTORS""; ""LIST OF ENTRIES""; ""Dictionary of Gnosis & Western Esotericism""; ""INDEX OF GROUPS AND ORGANIZATIONS""; ""INDEX OF PERSONS"" 606 $aOccultism$vDictionaries 606 $aOccultism$zEurope$vDictionaries 608 $aElectronic books. 615 0$aOccultism 615 0$aOccultism 676 $a35 701 $aHanegraaff$b Wouter J$0930267 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910458725103321 996 $aDictionary of gnosis & Western esotericism$92212835 997 $aUNINA LEADER 00673nam0-2200265 --450 001 9910584694703321 005 20220803165241.0 010 $a978-88-7168-509-0 100 $a20220803d2009----kmuy0itay5050 ba 101 0 $aita 102 $aIT 105 $a 001yy 200 1 $aZamel$fFranco Buffoni 210 $aMilano$cMarcos y Marcos$d[2009] 215 $a233 p.$d17 cm 225 1 $aMarcosUltra$v2 676 $a853.914$v21 700 1$aBuffoni,$bFranco$068722 801 0$aIT$bUNINA$gREICAT$2UNIMARC 901 $aBK 912 $a9910584694703321 952 $a853.914 BUF 1$b2021/1971$fFLFBC 959 $aFLFBC 996 $aZamel$92901187 997 $aUNINA LEADER 05345nam 2200685Ia 450 001 9911019196303321 005 20251116153005.0 010 $a9786612372230 010 $a9781282372238 010 $a1282372238 010 $a9783527621965 010 $a3527621962 010 $a9783527621972 010 $a3527621970 035 $a(CKB)1000000000441547 035 $a(EBL)481724 035 $a(SSID)ssj0000292340 035 $a(PQKBManifestationID)11228885 035 $a(PQKBTitleCode)TC0000292340 035 $a(PQKBWorkID)10269483 035 $a(PQKB)10010065 035 $a(MiAaPQ)EBC481724 035 $a(OCoLC)232611341 035 $a(Perlego)2756790 035 $a(EXLCZ)991000000000441547 100 $a20071029d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aComputational modeling for homogeneous and enzymatic catalysis $ea knowledge-base for designing efficient catalysts /$fedited by Keiji Morokuma and Djamaladdin G. Musaev 210 $aWeinheim $cWiley-VCH ;$aChichester $cJohn Wiley [distributor]$d2008 215 $a1 online resource (400 p.) 300 $aDescription based upon print version of record. 311 08$a9783527318438 311 08$a3527318437 320 $aIncludes bibliographical references and index. 327 $aComputational Modeling for Homogeneous and Enzymatic Catalysis; Contents; Preface; List of Contributors; 1 Computational Insights into the Structural Properties and Catalytic Functions of Selenoprotein Glutathione Peroxidase (GPx); 1.1 Introduction; 1.2 Catalytic Functions; 1.2.1 Peroxidase Activity; 1.2.2 Reductase Activity; 1.3 Computational Details; 1.3.1 Computational Methods; 1.3.2 Computational Models; 1.4 Results and Discussion; 1.4.1 Refinement of the Active Site; 1.4.2 Catalytic Functions: Peroxidase Activity 327 $a1.4.3 Catalytic Functions: Effect of the Surrounding Protein on the Peroxidase Activity1.4.3.1 Hydrogen Peroxide Coordination; 1.4.3.2 Formation of Selenenic Acid [E-Se-OH]; 1.4.4 Catalytic Functions: Reductase Activity; 1.4.4.1 Peroxynitrite/Peroxynitrous Acid (ONOO ?/ONOOH) Coordination; 1.4.4.2 Oxidation Pathway; 1.4.4.3 Nitration Pathways; 1.5 Summary; References; 2 A Comparison of Tetrapyrrole Cofactors in Nature and their Tuning by Axial Ligands; 2.1 Introduction; 2.2 Methodology; 2.3 Comparison of the Intrinsic Chemical Properties of the Tetrapyrroles; 2.3.1 Introduction 327 $a2.3.2 Spin States2.3.3 Tetrapyrroles Prefer Their Native Ions; 2.3.4 Cavity Size and Flexibility of the Tetrapyrroles; 2.3.5 Cytochrome-like Electron Transfer; 2.3.6 Stability of a Metal-Carbon Bond; 2.3.7 Metallation Reaction; 2.4 Tuning of Tetrapyrrole Structure and Function by Axial Ligands; 2.4.1 Introduction; 2.4.2 Importance of the Lower Axial Ligand for B(12) Chemistry; 2.4.3 Lower Axial Ligand in Cofactor F430; 2.4.4 Importance of Axial Ligands for the Globins; 2.4.5 Role of Axial Ligands for the Cytochromes; 2.4.6 Role of the Axial Ligand in Heme Enzymes 327 $a2.4.7 Tuning the His Ligand by Hydrogen Bonds in Heme Proteins2.4.8 Axial Ligand in Chlorophylls; 2.5 Concluding Remarks; References; 3 Modeling of Mechanisms for Metalloenzymes where Protons and Electrons Enter or Leave; 3.1 Introduction; 3.2 Energy Diagrams; 3.2.1 Photosystem II; 3.2.2 Cytochrome c Oxidase; 3.2.3 Nitric Oxide Reduction; 3.2.4 NiFe-hydrogenase; 3.2.5 Molybdenum CO Dehydrogenase; 3.3 Conclusions; References; 4 Principles of Dinitrogen Hydrogenation: Computational Insights; 4.1 Introduction 327 $a4.2 Reaction Mechanism of the Coordinated Dinitrogen Molecule in Di-zirconocene-N(2) Complexes with a Hydrogen Molecule4.2.1 Mechanism of the Reaction (3); 4.2.2 Mechanisms of the Reactions (4) and (5); 4.3 Factors Controlling the N(2) Coordination Modes in the Di-zirconocene-N(2) Complexes; 4.4 Why the [(?(5)-C(5)Me(n)H(5-n))(2)Ti](2)(?(2),?(2),?(2)-N(2)) Complex Cannot Add a H(2) Molecule to the Side-on Coordinated N(2), while its Zr- and Hf-analogs Can 327 $a4.4.1 Relative Stability of the Lowest Singlet (S) and Triplet (T) Electronic States of the Complexes [(?(5)-C(5)Me(n)H(5-n))(2)M](2)(?(2),?(2),?(2)-N(2)), II_M (for M = Ti, Zr, and Hf, and n = 0 and 4) 330 $aHere, the world's most active and productive computational scientists from academia and industry present established, effective and powerful tools for understanding catalysts. With its broad scope -- nitrogen fixation, polymerization, C-H bond activation, oxidations, biocatalysis and much more -- this book represents an extensive knowledge base for designing efficient catalysts, allowing readers to improve the performance of their own catalysts. 517 3 $aKnowledge-base for designing efficient catalysts 606 $aCatalysis$xComputer simulation 606 $aCatalysts 615 0$aCatalysis$xComputer simulation. 615 0$aCatalysts. 676 $a660.2995 701 $aMorokuma$b K$g(Keiji),$f1934-2017.$01890793 701 $aMusaev$b Djamaladdin G$01840964 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019196303321 996 $aComputational modeling for homogeneous and enzymatic catalysis$94533129 997 $aUNINA