مشخصات کتاب

Inorganic Reactions and Methods: The Formation of Bonds to C, Si, Ge, Sn, Pb (Part 1), Volume 9

ویرایش:  
 
سری: Inorganic Reactions and Methods 
ISBN (شابک) : 9780471186601, 9780470145234 
ناشر:  
سال نشر: 1991 
تعداد صفحات: 778 
زبان: English 
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) 
حجم فایل: 143 مگابایت 

در صورت تبدیل فایل کتاب Inorganic Reactions and Methods: The Formation of Bonds to C, Si, Ge, Sn, Pb (Part 1), Volume 9 به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.

توجه داشته باشید کتاب واکنش‌های معدنی و روش‌ها: تشکیل پیوند به C، Si، Ge، Sn، Pb (قسمت 1)، جلد 9 نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.

توضیحاتی درمورد کتاب به خارجی

For the first time the discipline of modern inorganic chemistry has been systematized according to a plan constructed by a council of editorial advisors and consultants, among them three Nobel laureates (E.O. Fischer, H. Taube and G. Wilkinson).

Rather than producing a collection of unrelated review articles, the series creates a framework which reflects the creative potential of this scientific discipline. Thus, it stimulates future development by identifying areas which are fruitful for further research.

The work is indexed in a unique way by a structured system which maximizes its usefulness to the reader. It augments the organization of the work by providing additional routes of access for specific compounds, reactions and other topics.Content:
Chapter 5.2.1 Introduction (pages 1–4): E. Hengge
Chapter 5.2.3.1.2 By Other Methods (page 4): E. Hengge
Chapter 5.2.3.1.3 Formation of High?Purity Silicon (pages 4–6): E. Hengge
Chapter 5.2.3.1.4 Electrochemical Formation of Compounds with Si?Si Bonds (Including Elemental Silicon) (pages 6–7): E. Hengge
Chapter 5.2.3.2 From Metal Silicides (pages 7–8): E. Hengge
Chapter 5.2.3.2.2 Formation of Oligosilanes (pages 8–9): E. Hengge
Chapter 5.2.3.2.3 Formation of Polymeric Compounds (pages 9–10): E. Hengge
Chapter 5.2.3.3 From Silicon Hydrides and Organosilicon Hydrides (page 11): M. A. Ring
Chapter 5.2.3.3.2 By Direct Photolysis (pages 11–13): M. A. Ring
Chapter 5.2.3.3.3 By Sensitized Photolysis (pages 13–15): M. A. Ring
Chapter 5.2.3.3.4 By Catalyzed Reactions (pages 15–16): M. A. Ring
Chapter 5.2.3.3.5 By Reaction with Silylmetallic Compounds (page 17): M. A. Ring
Chapter 5.2.3.4 From Silicon Halides and Organosilicon Halides (pages 17–18): M. A. Ring
Chapter 5.2.3.4.2 By Halide Elimination with Active Metals (pages 18–20): M. A. Ring
Chapter 5.2.3.4.3 By Reaction with Silylmetallics (pages 20–22): M. A. Ring
Chapter 5.2.3.4.4 By Catalyzed Disproportionation (pages 22–23): M. A. Ring
Chapter 5.2.3.4.5 By Reaction with Organomagnesium Halide Reagents (pages 23–24): M. A. Ring
Chapter 5.2.3.4.6 By the Action of Silent Electric Discharge (page 24): M. A. Ring
Chapter 5.2.3.4.7 By Mercury?Photosensitized Photolyses (pages 24–25): M. A. Ring
Chapter 5.2.3.5 From Bissilylmercury Compounds (pages 25–26): M. A. Ring
Chapter 5.2.3.5.2 By Photolysis (page 26): M. A. Ring
Chapter 5.2.3.6 From Organosilanes and Silicon Halides by Hydrogenolysis (pages 26–27): M. A. Ring
Chapter 5.2.3.7 From Silylenes (pages 28–29): M. A. Ring
Chapter 5.2.3.7.2 By Insertions into Bonds of Silicon to Hydrogen, Oxygen and Silicon (pages 29–33): M. A. Ring
Chapter 5.2.3.7.3 By Addition to SI=C (page 33): M. A. Ring
Chapter 5.2.3.8 In the Direct Reaction of Methyl Chloride with Silicon?Copper (pages 33–34): M. A. Ring
Chapter 5.2.4 Formation of the Germanium?Germanium Bond (pages 34–39): J. Satge and P. Riviere
Chapter 5.2.4.1.2 From Sulfides (page 39): J. Satge and P. Riviere
Chapter 5.2.4.1.3 By Other Syntheses (pages 39–43): J. Satge and P. Riviere
Chapter 5.2.4.1.4 Formation of High?Purity Germanium (pages 43–45): J. Satge and P. Riviere
Chapter 5.2.4.2 From Organogermanium Hydrides (pages 45–46): J. Satge and P. Riviere
Chapter 5.2.4.2.2 By Hydrogermolysis Reaction (pages 46–48): J. Satge and P. Riviere
Chapter 5.2.4.2.3 By Germanium Hydride Decomposition (page 48): J. Satge and P. Riviere
Chapter 5.2.4.3 From Ge(IV) Halides and Organogermanium(IV) Halides (page 49): J. Satge and P. Riviere
Chapter 5.2.4.3.2 By Electrochemical Reduction (pages 49–51): J. Satge and P. Riviere
Chapter 5.2.4.3.3 By Halide Elimination with Active Metals (pages 52–55): J. Satge and P. Riviere
Chapter 5.2.4.3.4 By Reaction with Germyl?Metal Reagents (pages 55–59): J. Satge and P. Riviere
Chapter 5.2.4.3.5 By Reaction with Organometallic Reagents (pages 59–61): J. Satge and P. Riviere
Chapter 5.2.4.4 From Germanium(II) Halides (pages 61–62): J. Satge and P. Riviere
Chapter 5.2.4.4.2 By Reaction with Organometallic Reagents (pages 62–64): J. Satge and P. Riviere
Chapter 5.2.4.5 From Germyl Compounds of Cadmium, Mercury, Thallium, Antimony and Bismuth (pages 64–66): J. Satge and P. Riviere
Chapter 5.2.4.6 From Germylenes (pages 66–68): J. Satge and P. Riviere
Chapter 5.2.4.6.2 By Insertions into Bonds of Germanium to Hydrogen, Halogen, Carbon, Oxygen, Sulfur, Nitrogen, Phosphorus and Germanium (pages 68–73): J. Satge and P. Riviere
Chapter 5.2.5 The Formation of the Tin–Tin Bond (pages 73–75): B. Mathiasch
Chapter 5.2.5.1.2 From Sulfides (page 75): B. Mathiasch
Chapter 5.2.5.1.3 By Other Syntheses (pages 75–76): B. Mathiasch
Chapter 5.2.5.1.4 Allotropy of Tin (pages 76–77): B. Mathiasch
Chapter 5.2.5.2 From Organotin Hydrides (pages 77–79): B. Mathiasch
Chapter 5.2.5.2.2 By Reaction with Organotin Halogen, Pseudohalogen, Chalcogen and Pnictogen Compounds (pages 79–82): B. Mathiasch
Chapter 5.2.5.2.3 By Reaction with Organometallic Compounds (pages 82–83): B. Mathiasch
Chapter 5.2.5.2.4 By Reaction with Reducible Organic Compounds (pages 83–84): B. Mathiasch
Chapter 5.2.5.3 From Organotin Halides (pages 84–85): B. Mathiasch
Chapter 5.2.5.3.2 By Halide Elimination with Active Metals (pages 85–86): B. Mathiasch
Chapter 5.2.5.3.3 By Reaction with Stannyl Metal Reagents (pages 86–88): B. Mathiasch
Chapter 5.2.5.3.4 By Reactions with Bulky Organometallic Reagents (pages 88–89): B. Mathiasch
Chapter 5.2.5.4 From Tin(II) Halides by Reaction with Organometallic Reagents (pages 89–90): B. Mathiasch
Chapter 5.2.5.5 From Bis(Stannyl) Compounds of Mercury (pages 90–92): B. Mathiasch
Chapter 5.2.5.6 From Stannylenes (pages 93–94): B. Mathiasch
Chapter 5.2.5.6.2 By Insertions into Bonds of Tin to Hydrogen, Carbon and Tin (pages 94–95): B. Mathiasch
Chapter 5.2.5.7 From Sodium?Tin Alloys by Reaction with Organic and Organometallic Compounds (pages 95–96): B. Mathiasch
Chapter 5.2.6 Formation of the Lead?Lead Bond (page 96): M. Drager and N. Kleiner
Chapter 5.2.6.1 In Metallic Lead (pages 96–97): M. Drager and N. Kleiner
Chapter 5.2.6.1.1 From Oxides (page 97): M. Drager and N. Kleiner
Chapter 5.2.6.1.2 From Sulfides (pages 97–98): M. Drager and N. Kleiner
Chapter 5.2.6.1.3 By Other Syntheses (pages 98–99): M. Drager and N. Kleiner
Chapter 5.2.6.2 From Lead (II) and Lead(IV) Salts by Reaction with Organometallic Reagents (pages 99–101): M. Drager and N. Kleiner
Chapter 5.2.6.3 From Organolead Hydrides (page 101): M. Drager and N. Kleiner
Chapter 5.2.6.4 From Organolead Halides (pages 101–102): M. Drager and N. Kleiner
Chapter 5.2.6.4.2 By Reaction with Plumbyl ? Metal Reagents (page 102): M. Drager and N. Kleiner
Chapter 5.2.6.5 From Organolead Hydroxides by Electrolysis (pages 102–103): M. Drager and N. Kleiner
Chapter 5.2.6.6 From Lead Alloys (page 103): M. Drager and N. Kleiner
Chapter 5.2.6.6.2 By Reaction with Cryptate Reagents (page 103): M. Drager and N. Kleiner
Chapter 5.2.6.7 By Other Syntheses (page 104): M. Drager and N. Kleiner
Chapter 5.2.6.7.2 By Reductive Processes (pages 104–105): M. Drager and N. Kleiner
Chapter 5.2.7 The Formation of the Carbon?Silicon Bond (pages 105–110): B. Kanner
Chapter 5.2.7.2.2 By Reaction with Aryl Halides (pages 110–112): B. Kanner
Chapter 5.2.7.2.3 By Reaction with Other Species (pages 112–113): B. Kanner
Chapter 5.2.7.3 From Silicon Halides (pages 113–138): P. P. Gaspar
Chapter 5.2.7.3.2 By Interaction with Organic Halides with Active Metals (pages 138–143): P. P. Gaspar
Chapter 5.2.7.3.3 By Interaction with Unsaturated Organic Derivatives and Active Metals (pages 143–159): P. P. Gaspar
Chapter 5.2.7.3.4 By Redistribution Reactions with Organosilanes (pages 159–161): P. P. Gaspar
Chapter 5.2.7.3.5 By Reaction with Hydrocarbons (page 161): P. P. Gaspar
Chapter 5.2.7.3.6 By Reaction with Diazoalkanes (pages 162–163): P. P. Gaspar
Chapter 5.2.7.4 From Silicon Alkoxides, Silicon Carboxylates or Siloxanes (pages 163–170): P. P. Gaspar
Chapter 5.2.7.4.2 By Interaction with Organic Halides and Active Metals (pages 170–173): P. P. Gaspar
Chapter 5.2.7.4.3 By Interaction with Unsaturated Organic Compounds (pages 173–176): P. P. Gaspar
Chapter 5.2.7.5 From Silicon Hydrides (pages 176–180): M. A. Ring
Chapter 5.2.7.5.2 By Reaction with Diazoalkanes or Other Carbenoids (pages 180–182): M. A. Ring
Chapter 5.2.7.5.3 By Reaction with Active Organometallics to Eliminate MH (pages 182–185): M. A. Ring
Chapter 5.2.7.5.4 From the Pyrolysis of Organohydrosilanes (page 185): M. A. Ring
Chapter 5.2.7.6 From Silylmetallics (pages 185–186): F. K. Cartledge and R. V. Piccione
Chapter 5.2.7.6.1 By Reaction with Organic Halides to Eliminate MX (pages 186–195): F. K. Cartledge and R. V. Piccione
Chapter 5.2.7.6.2 By Cleavage of Certain Ethers and Epoxides (pages 195–198): F. K. Cartledge and R. V. Piccione
Chapter 5.2.7.6.3 By Addition to Carbonyl Groups of CO2 and Other Acyl Derivatives (pages 198–202): F. K. Cartledge and R. V. Piccione
Chapter 5.2.7.6.4 By Addition to C—C Unsaturated Systems (pages 202–207): F. K. Cartledge and R. V. Piccione
Chapter 5.2.7.7 From Other Organosilanes by Exchange with Active Organometallics (pages 207–212): F. K. Cartledge and R. V. Piccione
Chapter 5.2.8 Formation of the Carbon?Germanium Bond (pages 212–215): B. Kanner
Chapter 5.2.8.2.2 By Reaction with Aryl Halides (pages 215–216): B. Kanner
Chapter 5.2.8.3 From Germanium Halides (DI? and Tetravalent) (page 216): J. Satge and P. Riviere
Chapter 5.2.8.3.1 By Reaction with Active Organometallics (pages 217–224): J. Satge and P. Riviere
Chapter 5.2.8.3.2 By Interaction with Organic Halides and Active Metals (pages 224–227): J. Satge and P. Riviere
Chapter 5.2.8.3.3 By Addition of Organic Halide to Germanium (II) Halides and Organohalogermylenes (pages 227–228): J. Satge and P. Riviere
Chapter 5.2.8.3.4 By Addition of Germylenes to Unsaturated Compounds (pages 228–232): J. Satge and P. Riviere
Chapter 5.2.8.3.5 By Redistribution Reactions with Organogermanes (pages 232–234): J. Satge and P. Riviere
Chapter 5.2.8.3.6 By Reaction with Diazoalkanes (pages 234–236): J. Satge and P. Riviere
Chapter 5.2.8.4 From Germanium Alkoxides, Germanium Carboxylates or Germanium Oxides (pages 236–237): J. Satge and P. Riviere
Chapter 5.2.8.4.1 By Reaction with Active Organometallics (pages 237–239): J. Satge and P. Riviere
Chapter 5.2.8.4.2 By Reaction with Organic Halides and Active Metals (page 239): J. Satge and P. Riviere
Chapter 5.2.8.5 From Germanium Hydrides (pages 240–251): J. Satge and P. Riviere
Chapter 5.2.8.5.2 By Reaction with Diazoderivatives or Other Carbenoides (pages 252–253): J. Satge and P. Riviere
Chapter 5.2.8.5.3 By Reaction with Active Organometallics to Eliminate MH (pages 254–256): J. Satge and P. Riviere
Chapter 5.2.8.6 From Germyimetallics (pages 256–257): F. Glockling
Chapter 5.2.8.6.1 By Reaction with Organic Halides to Eliminate HX (pages 257–261): F. Glockling
Chapter 5.2.8.6.2 By Reaction with Ethers (pages 261–262): F. Glockling
Chapter 5.2.8.6.3 By Addition to the Carbonyl Group of Co2 and Other Acyl Derivatives (pages 262–264): F. Glockling
Chapter 5.2.8.6.4 By Addition to Alkenes and Alkynes (pages 264–266): F. Glockling
Chapter 5.2.8.7 From Other Organogermanes by Exchange with Active Organometallics (pages 266–268): F. Glockling
Chapter 5.2.9 Formation of the Carbon?Tin Bond (pages 268–269): R. C. Poller
Chapter 5.2.9.2.1 By Reaction with Alkyl Halides (pages 269–272): R. C. Poller
Chapter 5.2.9.2.2 By Reaction with Alkyl Halides Having Alkenyl or Aryl Substituents (pages 272–273): R. C. Poller
Chapter 5.2.9.2.3 By Reaction with Alkyl Halides Having Other Substituents (pages 273–276): R. C. Poller
Chapter 5.2.9.2.4 By Electrolysis at a Tin Anode (pages 276–277): R. C. Poller
Chapter 5.2.9.2.5 By Electrolysis at a Tin Cathode (pages 277–278): R. C. Poller
Chapter 5.2.9.3 From Tin Halides (Di? and Tetravalent) (pages 278–311): P. G. Harrison
Chapter 5.2.9.3.2 Redistribution Reactions Involving Tetraorganostannanes and Tin(IV) Halides (pages 311–317): P. G. Harrison
Chapter 5.2.9.3.3 From Tin(II) Halides (pages 317–322): P. G. Harrison
Chapter 5.2.9.3.4 By Reaction with Diazoalkanes (pages 322–323): M. F. Lappert
Chapter 5.2.9.3.5 By Reaction with Another Carbon?Centered Protic Compound (pages 323–324): M. F. Lappert
Chapter 5.2.9.4 From Tin Alkoxides, Tin Carboxylates or Tin Oxides (pages 324–327): P. G. Harrison
Chapter 5.2.9.4.2 By Reaction with Terminal Acetylenes (page 327): P. G. Harrison
Chapter 5.2.9.4.3 By Decarboxylation of Organotin Carboxylates and Other Elimination Reactions (pages 328–329): P. G. Harrison
Chapter 5.2.9.4.4 By Addition to Carbon?Carbon Multiple Bonds (pages 329–330): P. G. Harrison
Chapter 5.2.9.4.5 By Transesterification (pages 331–332): P. G. Harrison
Chapter 5.2.9.5 From Tin Hydrides (pages 332–333): P. G. Harrison
Chapter 5.2.9.5.1 By Hydrostannation of Alkenes (pages 333–345): P. G. Harrison
Chapter 5.2.9.5.2 By Hydrostannation of Alkynes (pages 345–349): P. G. Harrison
Chapter 5.2.9.5.3 By Formation of Heterocyclic Compounds by Hydrostannation (pages 350–352): P. G. Harrison
Chapter 5.2.9.5.4 By Reaction with Diazoalkanes (page 352): P. G. Harrison
Chapter 5.2.9.6 From Organotin Amides (pages 353–354): M. F. Lappert
Chapter 5.2.9.6.1 By Insertion (page 355): M. F. Lappert
Chapter 5.2.9.6.2 By Reaction with a Terminal Acetylene (pages 356–357): M. F. Lappert
Chapter 5.2.9.6.3 By Reaction with a Cyclopentadiene (page 357): M. F. Lappert
Chapter 5.2.9.6.4 By Reaction with a Diazoalkane (pages 357–358): M. F. Lappert
Chapter 5.2.9.6.5 By Reaction with Another Carbon?Centered Protic Compound (pages 358–359): M. F. Lappert
Chapter 5.2.9.7 From Stannylmetallics (pages 359–360): F. Glockling
Chapter 5.2.9.7.1 By Reaction with Organic Halides to Eliminate MX (pages 360–365): F. Glockling
Chapter 5.2.9.7.2 By Addition to Alkenes and Alkynes (pages 365–366): F. Glockling
Chapter 5.2.9.7.3 By Cleavage of Ethers and Epoxides (page 367): F. Glockling
Chapter 5.2.9.8 From Other Organotins by Exchange with Active Organometallics (pages 367–369): F. Glockling
Chapter 5.2.10 Formation of the Carbon?Lead Bond (pages 370–375): F. Huber
Chapter 5.2.10.2.2 By Reaction with Aryl Halides (pages 375–376): F. Huber
Chapter 5.2.10.2.3 By Reaction with Other Species (page 376): F. Huber
Chapter 5.2.10.2.4 By Electrolysis of Sodium Tetraorganoaluminates at a Lead Anode (pages 377–379): F. Huber
Chapter 5.2.10.2.5 By the Action of Aryldiazonium Salts on Pb Metal (page 379): F. Huber
Chapter 5.2.10.3 From Lead Halides (Di? and Tetravalent) (pages 380–387): F. Huber
Chapter 5.2.10.3.2 By Interaction of Lead (II) Salts with an Active Organometallic and an Organic Halide (pages 387–388): F. Huber
Chapter 5.2.10.4 From Lead (II) Oxide, Lead Carboxylate or Plumbite Salts (page 389): B. Mauze
Chapter 5.2.10.4.2 By Reaction with an Active Organometallic (pages 389–394): B. Mauze
Chapter 5.2.10.5 From Organolead Hydrides (pages 394–396): P. G. Harrison
Chapter 5.2.10.6 From Organolead Amides (page 396): M. F. Lappert
Chapter 5.2.10.7 From Plumbylmetallics (page 397): F. Glockling
Chapter 5.2.10.7.1 By Reaction with Organic Halides to Eliminate MX (pages 397–399): F. Glockling
Chapter 5.2.10.7.2 By Addition to Alkenes and Alkynes (page 400): F. Glockling
Chapter 5.2.10.7.3 By Cleavage of Epoxides and Lactones (page 400): F. Glockling
Chapter 5.2.10.8 From Other Organoleads by Exchange with Active Organometallics (pages 400–404): F. Glockling
Chapter 5.2.11 Formation of Mixed Group?IVB–Group?IVB Element Bonds (Except Carbon–Group?IVB Bonds) (pages 404–405): M. Drager
Chapter 5.2.11.1 From the Elements (page 405): M. Drager
Chapter 5.2.11.1.2 Insilicides (pages 405–406): M. Drager
Chapter 5.2.11.1.3 In Germanides (page 406): M. Drager
Chapter 5.2.11.1.4 In Hydrides (pages 406–407): M. Drager
Chapter 5.2.11.2 From Group?IVB Halides (Di? and Tetravalent) (page 407): M. Drager
Chapter 5.2.11.2.2 By Reaction with a Group?IVB Element–Active Metal Reagent (pages 407–408): M. Drager
Chapter 5.2.11.3 From Group?IVB Hydrides (pages 408–409): M. Drager
Chapter 5.2.11.3.2 By Reaction with a Group?IVB Element Amide (page 409): M. Drager
Chapter 5.2.11.4 From Group?IVB Alkoxides and Carboxylates by Reaction with a Group?IVB Element?Active Metal Reagent (page 409): M. Drager
Chapter 5.2.11.5 From Mixed Group?IVB Element Mercurials, By Photolysis (page 410): M. Drager
Chapter 5.2.11.6 By Insertion of Silylenes, Germylenes, Stannylenes and Plumbylenes into Group?IVB–Hydrogen, –Halide and–Carbon Bonds (page 410): M. Drager

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