ورود به حساب

نام کاربری گذرواژه

گذرواژه را فراموش کردید؟ کلیک کنید

حساب کاربری ندارید؟ ساخت حساب

ساخت حساب کاربری

نام نام کاربری ایمیل شماره موبایل گذرواژه

برای ارتباط با ما می توانید از طریق شماره موبایل زیر از طریق تماس و پیامک با ما در ارتباط باشید


09117307688
09117179751

در صورت عدم پاسخ گویی از طریق پیامک با پشتیبان در ارتباط باشید

دسترسی نامحدود

برای کاربرانی که ثبت نام کرده اند

ضمانت بازگشت وجه

درصورت عدم همخوانی توضیحات با کتاب

پشتیبانی

از ساعت 7 صبح تا 10 شب

دانلود کتاب Inorganic syntheses. Volume 37

دانلود کتاب سنتزهای غیر آلی جلد 37

Inorganic syntheses. Volume 37

مشخصات کتاب

Inorganic syntheses. Volume 37

ویرایش:  
نویسندگان:   
سری:  
ISBN (شابک) : 9781119477730, 1119477735 
ناشر: Wiley Blackwell 
سال نشر: 2018 
تعداد صفحات: 280 
زبان: English 
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) 
حجم فایل: 3 مگابایت 

قیمت کتاب (تومان) : 42,000



کلمات کلیدی مربوط به کتاب سنتزهای غیر آلی جلد 37: ترکیبات معدنی -- سنتز



ثبت امتیاز به این کتاب

میانگین امتیاز به این کتاب :
       تعداد امتیاز دهندگان : 8


در صورت تبدیل فایل کتاب Inorganic syntheses. Volume 37 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 سنتزهای غیر آلی جلد 37 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



فهرست مطالب

Content: Note to Contributors and Checkers xv Toxic Substances and Laboratory Hazards xvii Preface xix Chapter One DIVALENT MANGANESE, IRON, AND COBALT BIS(TRIMETHYLSILYL)AMIDO DERIVATIVES AND THEIR TETRAHYDROFURAN COMPLEXES 1 1. Introduction 1 2. Bis{bis(trimethylsilyl)amido}iron(II) dimer: [Fe{N(SiMe3)2}2]2 4 A. Bis{bis(trimethylsilyl)amido}iron(II) dimer: [Fe{N(SiMe3)2}2]2 5 3. Bis{bis(trimethylsilyl)amido}cobalt(II) dimer, [Co{N(SiMe3)2}2]2,and bis{bis(trimethylsilyl)amido}(tetrahydrofuran)cobalt(II),Co{N(SiMe3)2}2(THF) 7 A. Bis{bis(trimethylsilyl)amido}cobalt(II) dimer: [Co{N(SiMe3)2}2]2 . 8 B. Bis{bis(trimethylsilyl)amido}(tetrahydrofuran)cobalt(II): Co{N(SiMe3)2}2(THF) 9 4. Bis{bis(trimethylsilyl)amido}manganese(II) dimer, [Mn{N(SiMe3)2}2]2, and its THF complexes Mn{N(SiMe3)2}2(THF) and Mn{N(SiMe3)2}2(THF)2 10 A. Bis{bis(trimethylsilyl)amido}(tetrahydrofuran)manganese(II),Mn{N(SiMe3)2}2(THF), and bis{bis(trimethylsilyl)amido} manganese(II) dimer, [Mn{N(SiMe3)2}2]2 11 B. Bis{bis(trimethylsilyl)amido}bis(tetrahydrofuran)manganese(II) 12 C. An alternative synthesis of Mn{N(SiMe3)2}2(THF) and [Mn{N(SiMe3)2}2]2 12 Chapter Two CALCIUM, STRONTIUM, GERMANIUM, TIN, AND LEAD BIS(TRIMETHYLSILYL)AMIDO DERIVATIVES AND 2,2,6,6- TETRAMETHYLPIPERIDIDO AND N-ISOPROPYLPHENYLAMIDO DERVATIVES OF POTASSIUM AND CALCIUM 15 1. Introduction 15 2. Potassium (2,2,6,6-tetramethylpiperidide), bis(2,2,6,6- tetramethylpiperidido) (N,N,N\',N\' -tetramethylethylenediamine)calcium(II), potassium (N-isopropylanilido), and bis(N-isopropylanilido) Tris (tetrahydrofuran)calcium(II) 18 A. Potassium 2,2,6,6-tetramethylpiperidide 19 B. Diiodotetrakis(tetrahydrofuran)calcium(II) 20 C. Bis(2,2,6,6-tetramethylpiperidido)(N,N,N\',N\'- tetramethylethylenediamine)calcium(II) 20 D. Potassium N-{isopropyl(phenyl)amide} (Potassium N-isopropylanilide) 21 E. Bis{<
!-- -->
N-isopropyl(phenyl)amido}tris(tetrahydrofuran)calcium(II) 22 F. Bis[{bis(tetrahydrofuran)potassium}bis{ -N(isopropyl)(phenyl) amido}]calcium(II) 22 3. Bis{bis(trimethylsilyl)amido}calcium(II) dimer, [Ca{N(SiMe3)2}2]2, and bis {bis(trimethylsilyl)amido}strontium(II) dimer, [Sr{N(SiMe3)2}2]2 24 A. Bis{bis(trimethylsilyl)amido}calcium(II) dimer, [Ca{N(SiMe3)2}2]2,and bis{bis(trimethylsilyl)amido}strontium(II) dimer, [Sr{N(SiMe3)2}2]2 25 4. Divalent Group 14 metal bis(trimethylsilylamides), M{N(SiMe3)2}2 (M = Ge, Sn, Pb) 26 A. Bis{bis(trimethylsilyl)amido}germanium(II), Ge{N(SiMe3)2}2 27 B. Bis{bis(trimethylsilyl)amido}tin(II), Sn{N(SiMe3)2}2 28 C. Bis{bis(trimethylsilyl)amido}lead(II), Pb{N(SiMe3)2}2 29 Chapter Three COMPOUNDS WITH Zn-Zn AND Mg-Mg BONDS: DECAMETHYLDIZINCOCENE AND ss-DIKETIMINATO COMPLEXES OF MAGNESIUM(I) AND (II) 33 1. Introduction 33 2. Pentamethylcyclopentadienyl zinc(I) dimer, {Zn( 5-C5Me5)}2 37 A. Pentamethylcyclopentadienyl potassium 38 B. Bis(pentamethylcyclopentadienyl)zinc(II) 38 C. Bis(pentamethylcyclopentadienyl)dizinc(I) 39 3. ss-diketiminato complexes of magnesium(I)/(II) 40 A. {2,4-bis-(2,6-diisopropylphenylimido)pentyl}(diethylether) iodomagnesium(II), {HC(CMeNC6H3-2,6-Pri 2)2}MgI(OEt2) 41 B. {2,4-bis-(mesitylimido)pentyl}(diethylether) iodidomagnesium(II),{HC(CMeNC6H2-2,4,6-Me3)2}MgI(OEt2) 42 C. Bis{2,4-bis-(2,6-diisopropylphenylimido)pentyl}dimagnesium(I) [{HC(CMeNC6H3-2,6-Pri 2)2}2Mg]2 43 D. Bis{2,4-bis-(mesitylimido)pentyl}dimagnesium(I), [{HC(CMeN(C6H2-2,4,6-Me3)}Mg]2 44 Chapter Four STERICALLY CROWDED - AND -BONDED METAL ARYL COMPLEXES 47 1. Introduction 47 2. Dimesityliron(II) dimer and dimesityldipyridineiron(II) (Mes = Mesityl = C6H2-2,4,6-Me3) 50 A. Tetramesityldiiron(II) dimer (FeMes2)2 (Mes = 2,4,6-trimethylphenyl) 51 B. Dimesityldi(pyridine)iron(II) FeMes2py2 (py = C5H5N) 54 3. Homoleptic, two-coordinate open-shell 2,6-dimesitylphenyl complexes of lithium, manganese, iron, and cobalt 56 A. 1-Iodo-2,6-bis(2,4,6-trimethylphenyl)benzene, 2,6-dimesitylphenyl iodide 57 B. Bis{ -2,6-bis(2,4,6-trimethylphenyl)phenyl}dilithium, 2,6-dimesitylphenyllithium dimer 58 C. Bis{2,6-bis(2,4,6-trimethylphenyl)phenyl}manganese(II), (bis(2,6-dimesitylphenyl)manganese(II)) 59 D. Bis{2,6-bis(2,4,6-trimethylphenyl)phenyl}iron(II), bis(2,6-dimesitylphenyl)iron(II) 59 E. Bis{2,6-bis(2,4,6-trimethylphenyl)phenyl}cobalt(II),bis(2,6-dimesitylphenyl)cobalt(II) 60 4. Monomeric group 14 diaryls bis{2,6-bis(2,4,6-trimethylphenyl)phenyl} germanium(II), tin(II), or lead(II), M{C6H3-2,6-Mes2)2 and bis{2,6-bis(2,6- diisopropylphenyl)phenyl}germanium(II), tin(II), or lead(II), M{C6H3-2,6-Dipp2}2 (M = Ge, Sn, or Pb
Mes = C6H2-2,4,6-Me3
Dipp = C6H3-2,6-Pri2) 61 5. m-terphenylgallium chloride complexes 65 A. {Bis(diethylether)lithium}{trichlorido(2,6-diphenyl)phenylgallate}, {Li(Et2O)2}{(C6H3-2,6-Ph2)GaCl3} 66 B. Chlorido{bis(2,6-dimesitylphenyl)}gallium, (2,6-Mes2C6H3)2GaCl 67 6. {(18-crown-6)bis(tetrahydrofuran)potassium}{bis(1,2,3,4- 4-anthracene)metallates} of cobalt(-I) and iron(-I),{K(18-crown-6)(THF)2} {M( 4-C14H10)2}, M= Co, Fe 67 A. {(18-crown-6)bis(tetrahydrofuran)potassium}{bis(1,2,3,4- 4-anthracene)cobaltate}, {K(18-crown-6)(THF)2}{Co(C14H10)2} 69 B. {(18-crown-6)bis(tetrahydrofuran)potassium}{bis(1,2,3,4- 4-anthracene)ferrate}, {K(18-crown-6)(THF)2}{Fe(C14H10)2} 70 7. {Bis(1,2-dimethoxyethane)potassium}{bis(1,2,3,4- 4-anthracene) cobaltate}, {K(DME)2}{Co( 4-C14H10)2} 72 8. Cyclopentadienyl and pentamethylcyclopentadienyl naphthalene ferrates 76 A. Bis(tetrahydrofuran)lithium cyclopentadienyl(1,2,3,4- 4-napthalene) ferrate, [{Li(thf)2}{CpFe( 4-C10H8)}] 78 B. (18-crown-6)potassium pentamethylcyclopentadienyl(1,2,3,4- 4- napthalene)ferrate, [K(18-crown-6){Cp Fe( 4-C10H8)}] 79 Chapter Five TERPHENYL LIGANDS AND COMPLEXES 85 1. Introduction 85 2. m-Terphenyl iodo and lithium reagents featuring 2,6-bis-(2,6- diisopropylphenyl) substitution patterns and an m-terphenyl lithium etherate featuring the 2,6-bis-(2,4,6-triisopropylphenyl) substitution pattern 89 A. 1-bromo-2,6-diisopropylbenzene, 1-Br-2,6-Pri2C6H3
DippBr) 90 B. 1-iodo-2,6-bis(2,6-diisopropylphenyl)benzene (IC6H3-2,6-Dipp2) 92 C. Bis{2,6-bis(2,6-diisopropylphenyl)phenyl}dilithium,(LiC6H3-2,6-Dipp2)2 94 D. 2,6-bis(2,6-diisopropylphenyl)phenyllithiumetherate 95 E. 2,6-bis(2,4,6-triisopropylphenyl)phenyllithiumetherate{(Et2O)LiC6H3-2,6-Trip2} 96 3. 2,6-dimesitylaniline (H2NC6H3-2,6-Mes2) and 2,6-bis(2,4,6- triisopropylphenyl)aniline (H2NC6H3-2,6-Trip2) 98 A. 2,6-dimesitylphenylazide, 2,6-Mes2C6H3N 99 B. 2,6-dimesitylaniline, 2,6-Mes2C6H3NH2 100 C. 2,6-bis(2,4,6-triisopropylphenyl)iodobenzene, 2,6-Trip2C6H3I 101 D. 2,6-bis(2,4,6-triisopropylphenyl)azidobenzene,2,6-Trip2C6H3N3 102 E. 2,6-bis(2,4,6-triisopropylphenyl)aniline, 2,6-Trip2C6H3NH2 103 4. Bis-2,6-(2,6-diisopropylphenyl)aniline 105 A. 1-azido-bis-2,6-(2,6-diisopropylphenyl)benzene,2,6-Dipp2H3C6N3 106 B. Bis-2,6-(2,6-diisopropylphenyl)aniline, 2,6-Dipp2H3C6NH2 107 5. Bis-2,6-(2,4,6-trimethylphenyl)phenylformamide and isocyanide,Bis-2,6-(2,6-diisopropylphenyl)phenylformamide and isocyanide 109 A. 2,6-dimesitylphenyl formamide {2,6-Mes2H3C6N(H)C(O)H} 110 B. 2,6-dimesitylphenyl isocyanide (2,6-Mes2H3C6NC) 111 C. 2,6-bis-(diisopropylphenyl)phenyl formamide{2,6-Dipp2H3C6N(H)C(O)H} 112 D. 2,6-bis-(diisopropylphenyl)phenyl isocyanide (2,6-Dipp2H3C6NC) 113 6. Synthesis of the terphenylthiols: 2,6-bis(2,6-diisopropylphenyl)phenylthiol,2,6-bis(2,4,6-triisopropylphenyl)phenylthiol, and bis{2,6-bis(2,4,6-triisopropylphenyl)phenylthiolato}dilithium 116 A. 2,6-bis(2,6-diisopropylphenyl)phenylthiol 117 B. 2,6-bis(2,4,6-triisopropylphenyl)phenylthiol 118 C. Bis{2,6-bis(2,4,6-triisopropylphenyl)phenylthiolato}dilithium 119 7. Sterically encumbered terphenols: 2,6-bis(2,4,6-trimethylphenyl)phenol and 2,6-bis(2,6-diisopropylphenyl)phenol 120 A. 2,6-bis(2,6-diisopropylphenyl)phenol 121 B. Bis(2,4,6-trimethylphenyl)phenol 121 Chapter Six SYNTHETIC ROUTES TO WHITE PHOSPHORUS (P4) AND ARSENIC TRIPHOSPHIDE (AsP3) 123 1. Introduction 123 2. Facile preparation of white phosphorus from red phosphorus:Preparation A 125 3. Synthesis of white phosphorus (P4) from red phosphorus:Preparation B 127 4. Arsenic triphosphide, AsP3 130 A. Tris(2,6-diisopropylphenoxy)niobiumdichloride {Cl2Nb(ODipp)3} and Tris(2,6-diisopropylphenoxy)niobiumdichloride(tetrahydrofuran) {Cl2Nb(ODipp)3(THF)} 131 B. {Na(THF)3}{P3Nb(ODipp)3} 132 C. Arsenic Triphosphide AsP3 133 Chapter Seven SYNTHETIC ROUTES TO PHOSPHIDO AND ARSENIDO DERIVATIVES OF THE GROUP 13 METALS ALUMINUM, GALLIUM, AND INDIUM, TRIS(TERT-BUTYL)GALLIUM AND ITS REACTIONS WITH AMMONIA, AND THE ALUMINUM(I) SPECIES PENTAMETHYLCYCLOPENTADIENYL ALUMINUM TETRAMER 135 1. Introduction 135 2. Dinuclear phosphido and arsenido derivatives of aluminum, gallium, and indium {Me2M( -EBut2)}2, M= Al, Ga, In
E = P, As 137 A. Preparation of {Me2M( -EBut2)}2 Complexes: M= Al,Ga, In
E = P, As 138 3. Tris(tert-butyl)gallane, its ammonia complex, and the amidobis(tert-butyl)gallane trimer tris( -amido)hexa(tert-butyl)trigallium 140 A. Tri-tert-butylgallane 141 B. Ammonia complex of tri-tert-butylgallane 142 C. Tris( -amido)hexa-tert-butyltrigallium: The trimer {But2Ga ( -NH2)}3 143 4. Reductive elimination as a convenient pathway to tetrameric ( 5-pentamethylcyclopentadienyl)aluminum(I) {(AlCp )4} (Cp = 5-C5Me5) 144 A. Potassium pentamethylcyclopentadienide KCp 146 B. Bis(pentamethylcyclopentadienyl)aluminumhydride (Cp 2AlH) 146 C. Tetrameric ( 5-pentamethylcyclopentadienyl)aluminum(I){(AlCp )4} 147 5. A facile synthesis of tetrameric (n5-pentamethylycycloclopentadienyl) aluminum(I) {Al(n5-C5Me5)}4 147 A. (n5-pentamethylcyclopentadienyl)aluminumdichloride 149 B. Tetrameric (n5-pentamethylcyclopentadienyl)aluminum(I) (AlCp )4 149 6. Tris(pentafluorophenyl)aluminum(toluene): Al(C6F5)3(C7H8) 150 A. Tris(pentafluorophenyl)aluminum(toluene) 151 Chapter Eight SYNTHESIS OF SELECTED TRANSITION METAL AND MAIN GROUP COMPOUNDS WITH SYNTHETIC APPLICATIONS 155 1. Introduction 155 2. Synthesis of gold(I) and gold(II) amidinate complexes 157 A. Synthesis of gold(I) amidinate complexes 158 B. Synthesis of gold(II) amidinate complexes 161 3. A nickel-iron thiolate and its hydride 166 A. (1,2-bis(diphenylphosphino)ethane)(1,3-propanedithiolato) nickel(II) 167 B. (1,2-bis(diphenylphosphino)ethane)nickel(I)( -1,3- propanedithiolato)tricarbonyliron(I) 168 C. (1,2-bis(diphenylphosphino)ethane)nickel(II)( -hydrido)( -1,3-propanedithiolato)tricarbonyliron(II) tetrafluoroborate 169 4. Dimethyl sulfoxide and organophosphine complexes of ruthenium(II) halides 171 A. cis-tetrakis(dimethylsulfoxide)ruthenium(II)dichloride 172 B. cis-bis{1,2-bis(diphenylphosphino)ethane}ruthenium(II) dichloride 174 C. Bis{1,2-bis(diphenylphosphino)ethane}chlororuthenium(II) hexafluorophosphate 174 D. trans-bis{1,2-bis(diphenylphosphino)ethane}ruthenium(II) dichloride 176 5. Synthesis of {CrIII(NCMe)6}(BF4)3 and {CrIII(NCMe)5F} (BF4)2*MeCN 177 A. Hexakis(acetonitrile)chromium(III) tetrafluoroborate, {CrIII(NCMe)6}(BF4)3 177 B. Pentakis(acetonitrile)fluorido chromium(III) tetrafluoroborate, {CrIIIF(NCMe)5}(BF4)2 178 6. (1R,2R-diaminocyclohexane)oxalatoplatinum(II), oxaliplatin 179 7. Tris(dibenzylideneacetone)dipalladium(0) 183 A. Synthesis of Pd2dba3 CHCl3 185 B. Purity determination and repurification of Pd2dba3 186 C. Stability 187 8. Tetraalkylammonium salts of tetra(fluoroaryl)borate anions 188 A. Tetraalkylammonium salts of [B(C6F5)4] 189 B. Tetraalkylammonium salts of [B{C6H3-3,5-(CF3)2}4] 191 9. Titanium tris(N-tert-butyl, 3,5-dimethylanilide) 193 10. Tetrachlorido(tetramethylethylenediamine)tantalum(IV),TaCl4(TMEDA) 196 A. Tetrachlorido(tetramethylethyenediamine)tantalum(IV),TaCl4(TMEDA) 197 11. Synthesis of 1,3,5-tri-tert-butylcyclopenta-1,3-diene and its metal complexes Na{1,2,4-(Me3C)3C5H2} and Mg{ 5-1,2,4-(Me3C)3C5H2}2 199 A. Method A (Phase Transfer) 199 B. Method B (Grignard Procedure) 201 C. Sodium(1,2,4-tri-tert-butyl)cyclopentadienide 203 D. Magnesium(II)bis(1,2,4-tri-tert-butyl)cyclopentadienide 203 Cumulative Contributor Index 205 Cumulative Subject Index 215 Cumulative Formula Index 245




نظرات کاربران