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135   $aur|n|---|||||
181   $ctxt
182   $cc
183   $acr
200 00$aFerrocenes$b[electronic resource] $ecompounds, properties and applications /$fElisabeth S. Phillips, editor
210   $aNew York $cNova Science Publishers$dc2011
215   $a1 online resource (413 p.)
225  0$aChemical engineering methods and technology
300   $aDescription based upon print version of record.
311   $a1-61761-880-2 
320   $aIncludes bibliographical references and index.
327   $a""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS ""; ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS""; ""CONTENTS""; ""PREFACE""; ""SYNTHESIS OF PRISTINE AND DOPED CARBON NANOTUBES USING FERROCENE""; ""ABSTRACT ""; ""INTRODUCTION ""; ""STRUCTURE AND PROPERTIES OF FERROCENE ""; ""STRUCTURE AND BONDING ""; ""SYNTHESIS OF PRISTINE CARBON NANOTUBES ""; ""SYNTHESIS OF DOPED CARBON NANOTUBES""; ""CONCLUSION ""; ""REFERENCES ""; ""USE OF FERROCENE AND FERROCENE ADMIXED PRECURSORS FOR THE SYNTHESIS  OF CARBON NANOTUBES""; ""ABSTRACT ""; ""1. INTRODUCTION""
327   $a""2. SYNTHESIS OF CNTS USING FERROCENE """"3. SYNTHESIS OF CNTS BY FERROCENE  AND HYDROCARBON MIXTURE ""; ""3.1. Synthesis of CNTs by Ferrocene and Gaseous Hydrocarbon""; ""3.2. Synthesis of CNTs by Ferrocene and Liquid Hydrocarbon  ""; ""3.2.1. CVD of Ferrocene - Liquid Hydrocarbon Through Syringe Pump""; ""3. 2.2. Spray Assisted CVD Method ""; ""3.2.3. Aerosol and Nebulized Spray Assisted CVD Method""; ""4. SYNTHESIS OF CNTS USING FERROCENE  AND NATURAL PRECURSOR""; ""5. SYNTHESIS OF CNTS USING FERROCENE AND OTHER  CARBON SOURCES""; ""6. SUMMARY ""; ""ACKNOWLEDGMENTS ""; ""REFERENCES ""
327   $a""TRANSITION-METAL CATALYZED REACTIONS  IN THE SYNTHESIS OF FERROCENE DERIVATIVES""""ABSTRACT ""; ""1. INTRODUCTION ""; ""2. HOMOGENEOUS CATALYTIC HYDROGENATION  OF FERROCENE DERIVATIVES ""; ""3. SYNTHESIS OF CHIRAL DIOLS BY ASYMMETRIC DIHYDROXYLATION OF FERROCENYL ALKENES ""; ""4. HOMOGENEOUS CATALYTIC HYDROSILYLATION  OF FERROCENE DERIVATIVES ""; ""5. CARBON-CARBON BOND-FORMING REACTIONS ""; ""5.1. Heck Reactions of Ferrocenyl Substrates ""; ""5.2. Cross-Coupling Reactions ""; ""5.2.1. Stille Coupling ""; ""5.2.2. Suzuki Coupling ""; ""5.2.3. Negishi Coupling ""
327   $a""5.2.4. Cross-Coupling of Organomercurials """"5.2.5. Other Coupling Reactions with Organometallic Reagents""; ""5.2.6. Sonogashira Coupling ""; ""5.3. Metathesis Reactions ""; ""5.3.1. Ring-Closing Metathesis Reactions ""; ""5.3.2. Ring-Opening Metathesis Polymerization ""; ""6. C-HETEROATOM COUPLING REACTIONS  OF FERROCENE DERIVATIVES ""; ""7. RING-OPENING POLYMERIZATION REACTIONS ""; ""8. COPPER CATALYZED AZIDE-ALKYNE CYCLOADDITION ""; ""9. CARBONYLATION REACTIONS LEADING TO CARBOXYLIC ACID DERIVATIVES AND CARBONYL COMPOUNDS ""; ""9.1. Palladium-Catalyzed Aminocarbonylation ""
327   $a""9.2. Carbonylative Coupling Reactions """"10. MISCELLANEOUS REACTIONS ""; ""CONCLUSION ""; ""REFERENCES ""; ""EXPLOITING FERROCENE TO DEVELOP SYNTHETIC MOLECULAR MACHINES ""; ""ABSTRACT ""; ""1. INTRODUCTION""; ""2. FERROCENE HOST-GUEST CHEMISTRY AND STIMULI RESPONSIVE HOST-GUEST SYSTEMS ""; ""2.1. Ferrocene Host-Guest Chemistry ""; ""2.2 Stimuli Responsive Host-Guest Systems Containing Ferrocene""; ""3. STIMULI RESPONSIVE INTERLOCKED ARCHITECTURES CONTAINING FERROCENE ""; ""3.1. Introduction to Mechanically Interlocked Architectures ""
327   $a""3.2 Ferrocene Containing Mechanically Interlocked Architectures""
410  0$aChemical Engineering Methods and Technology
606   $aFerrocene
606   $aOrganoiron compounds
615  0$aFerrocene.
615  0$aOrganoiron compounds.
676   $a547/.05621
701   $aPhillips$b Elisabeth S$01541762
801  0$bMiAaPQ
801  1$bMiAaPQ
801  2$bMiAaPQ
906   $aBOOK
912   $a9910790033003321
996   $aFerrocenes$93794126
997   $aUNINA