2 Homometallic Alkoxides

More documents

Recommendations

Info

327 Table 4.15 <strong>Alkoxides</strong> of copper, silver, and gold M–O Bond lengths ( ˚A) Metal Bond angles ( Ž ) Compound coordination Terminal Bridging MOC � Reference [Cu4⊲ -OBu t ⊳4] 2 – 1.813–1.882 (10) av. 1.852 119.8–127.3 420 [Cu2⊲ -OBu t ⊳2⊲PPh3⊳2] 3 – 1.960, 1.996 (4) 126.9, 132.1 421 [Cu4⊲ -OSiPh3⊳4] 2 – 1.833–1.856 (4) av. 1.844 117.8–134.7 422 [Cu2⊲ -OSiPh3⊳2⊲PMe2Ph⊳2] [Cu4f -OSiPh⊲OBu 3 – 1.946, 2.046 (2) 123.2, 133.5 422 t ⊳2g4] 2 – 1.827–1.844 (5) av. 1.835 131.9, 132.1 423 [Cu2f -O⊲CH2⊳4NDC(Me)CH2C⊲CF3⊳2Og2] 4 – 1.892–1.924 (2) av. 1.905 121.2, 127.2 424 [Cu2f -O⊲CH2⊳3NDC(Me)CH2C⊲CF3⊳2Og2] 4 – 1.876–1.926 (2) av. 1.899 122.5, 128.7 424 [Cu2f -OC⊲CF3⊳2CH2C(Me)DN 4 1.857–1.876 (7) – 123.9–126.2 425 ⊲CH2⊳5NDC(Me)CH 2C⊲CF3⊳2Og2] av. 1.864 [CufOC⊲CF3⊳2CH2CHNHRg2] 4 1.906, 1.934 (8) – 118.8, 120.2 426 R D menthyl [CufOC⊲CF3⊳2⊲OH⊳g4] 2 4 av. 1.933 (6) – – 427 [CufO2C⊲CF3⊳2gL] 5 1.977, 1.999 (4) – 90.9, 91.4 406 L D cyclo-N DC(Me)CH 2C⊲Me⊳2NH⊲C3H6⊳NH⊲C3H6⊳ [CufOC⊲CF3⊳2OC⊲CF3⊳2Og⊲Me2NC2H4NMe2⊳] 4 1.890–1.895 (4) – 120.8–121.7 428 av. 1.893 (continued overleaf )
328 Table 4.15 (Continued) M–O Bond lengths ( ˚A) Metal Bond angles ⊲Ž⊳ Compound coordination Terminal Bridging MOC � Reference [CufOC⊲CF3⊳2CH2C(O)DCHC⊲CF3⊳2OHg 4 1.874, 1.881 (8) – 121.0, 124.0 407 ⊲Me2NC2H4NMe2⊳] [CufOCH2C⊲Me⊳2NH2g2] 4 1.916 (3) – 112.5 429 [CufOCH(Me)CH2NMe2g2] 4 1.865 (3) – – 430 [CufOCH2CH2N(Me)CH2CH2NMe2g2] [f⊲CF3⊳3COgfCu⊲ -OBu 5 1.887, 1.892 (17) – – 430 t ⊳2Cug3fOC⊲CF3⊳3g] 3 and 4 1.797 (5) 1.86 short 1.95 long 120.7–138.5 431 [CufOCH⊲CF3⊳2g2⊲Me2NC2H4NMe2⊳] 4 1.895, 1.910 (3) – 116.1, 120.9 432 [CufOCMe⊲CF3⊳2g2⊲Me2NC2H4NMe2⊳] 4 1.884 (3) – 125.5 432 0 [Cu4⊲ 3, -OC2H4OPr i ⊳4(acac) 4] 5 1.901–1.921 (acac) av. 1.910 1.939–1.953 (3) (alkoxo) av. 1.948 – 433 [Cu4⊲ - 4-L⊳2(prz) 4 (MeOH) 2] 2C L D MeOC⊲C5H4N⊳2O; prz D pyrazolate [Cu3f -OCH⊲CH2NMe2⊳2g4(MeOH)Cl2] 4 and 5 5 2.396 (4) (MeOH) 1.948 (7) (alkoxo) 2.06 (1) (MeOH) 1.934, 1.964 (4) 1.948, 1.984 (6) 115.8, 117.4 115.0 (t) 111.6, 112.5 (b) 434 435 [Cu4⊲ -OMe⊳4⊲ , 2-O2CMe⊳4] 4 1.933–1.966 (3) 1.914–1.920 (3) – 436 (acetate) (MeO) av. 1.948 av. 1.917 b D bridging, t D terminal.
Page 1 and 2:
Alkoxo and Aryloxo Derivatives of M
Page 3 and 4:
1 Introduction In 1978 the book ent
Page 5 and 6:
1 INTRODUCTION 2 Homometallic Alkox
Page 7 and 8:
Homometallic Alkoxides 5 to complet
Page 9 and 10:
Table 2.1 (Continued) Homometallic
Page 11 and 12:
Page 13 and 14:
Page 15 and 16:
Page 17 and 18:
Homometallic Alkoxides 15 reactivit
Page 19 and 20:
Homometallic Alkoxides 17 By contra
Page 21 and 22:
Homometallic Alkoxides 19 2.3 React
Page 23 and 24:
Homometallic Alkoxides 21 has been
Page 25 and 26:
Homometallic Alkoxides 23 obtain on
Page 27 and 28:
y Evans and co-workers: 160,161 Hom
Page 29 and 30:
Homometallic Alkoxides 27 The heter
Page 31 and 32:
Homometallic Alkoxides 29 not conve
Page 33 and 34:
Homometallic Alkoxides 31 In view o
Page 35 and 36:
2.7.2 Steric Factors Homometallic A
Page 37 and 38:
Homometallic Alkoxides 35 (b) When
Page 39 and 40:
Homometallic Alkoxides 37 2.8 Trans
Page 41 and 42:
Homometallic Alkoxides 39 with orga
Page 43 and 44:
2.9.1.1 Alkoxides of Be, Mg, Ca, Sr
Page 45 and 46:
MfN⊲SiMe3⊳2g2thfx C2HOR, Cpy !C
Page 47 and 48:
Homometallic Alkoxides 45 2.10 Misc
Page 49 and 50:
Zr⊲CH2Bu t ⊳4 C 4RfOH benzene !
Page 51 and 52:
2.10.5 By Insertion of Oxygen into
Page 53 and 54:
Homometallic Alkoxides 51 First hom
Page 55 and 56:
O M R M OR M OR RO M (M = Tl; R = M
Page 57 and 58:
Homometallic Alkoxides 55 3. Nuclea
Page 59 and 60:
Homometallic Alkoxides 57 explain t
Page 61 and 62:
Decomposition (%) 100 80 60 40 20 0
Page 63 and 64:
Table 2.6 Volatilities of tetravale
Page 65 and 66:
Homometallic Alkoxides 63 deduced t
Page 67 and 68:
Table 2.10 Vapour pressure of Ti, Z
Page 69 and 70:
Homometallic Alkoxides 67 Table 2.1
Page 71 and 72:
3.2.10 Alkoxides of Later 3d Metals
Page 73 and 74:
Homometallic Alkoxides 71 Table 2.1
Page 75 and 76:
Homometallic Alkoxides 73 affected
Page 77 and 78:
Homometallic Alkoxides 75 the range
Page 79 and 80:
Homometallic Alkoxides 77 several c
Page 81 and 82:
Page 83 and 84:
Homometallic Alkoxides 81 In toluen
Page 85 and 86:
Bu t O Bu t O Bu t O Th O O Bu O t
Page 87 and 88:
Homometallic Alkoxides 85 1H NMR st
Page 89 and 90:
Homometallic Alkoxides 87 septet wa
Page 91 and 92:
Homometallic Alkoxides 89 experimen
Page 93 and 94:
Table 2.21 1 H NMR spectra of Al4(O
Page 95 and 96:
Homometallic Alkoxides 93 3.5 Elect
Page 97 and 98:
Homometallic Alkoxides 95 ligand fi
Page 99 and 100:
Homometallic Alkoxides 97 susceptib
Page 101 and 102:
10 −1 /xM 12 10 −200 −100 0 [
Page 103 and 104:
Homometallic Alkoxides 101 alkoxide
Page 105 and 106:
Homometallic Alkoxides 103 fragment
Page 107 and 108:
Homometallic Alkoxides 105 The mass
Page 109 and 110:
Homometallic Alkoxides 107 [Al⊲OP
Page 111 and 112:
Homometallic Alkoxides 109 Under ca
Page 113 and 114:
4.3.2 Phenol-Alcohol Exchange React
Page 115 and 116:
4.4 Reactions with Alkanolamines Ho
Page 117 and 118:
Homometallic Alkoxides 115 R D Pr i
Page 119 and 120:
Homometallic Alkoxides 117 La(OPr i
Page 121 and 122:
Homometallic Alkoxides 119 with the
Page 123 and 124:
Homometallic Alkoxides 121 about 1.
Page 125 and 126:
Homometallic Alkoxides 123 concentr
Page 127 and 128:
Homometallic Alkoxides 125 and othe
Page 129 and 130:
Homometallic Alkoxides 127 Interest
Page 131 and 132:
OH Monofunctional bidentate HC N R
Page 133 and 134:
Homometallic Alkoxides 131 metal al
Page 135 and 136:
Homometallic Alkoxides 133 which yi
Page 137 and 138:
shown in Eq. (2.286): O Mo2(OEt)6 H
Page 139 and 140:
Homometallic Alkoxides 137 Phenyl i
Page 141 and 142:
Homometallic Alkoxides 139 The 1990
Page 143 and 144:
Eqs (2.312)-(2.315): where R D l-ad
Page 145 and 146:
Homometallic Alkoxides 143 On the b
Page 147 and 148:
Homometallic Alkoxides 145 The form
Page 149 and 150:
Homometallic Alkoxides 147 On furth
Page 151 and 152:
4.16 Interactions Between Two Diffe
Page 153 and 154:
4Mo2(OPr i )6 + 18CO (excess) Homom
Page 155 and 156:
isolobality of CR 0 and W⊲OR⊳3
Page 157 and 158:
W2(OR)8 (R = CH2Bu t ) + CO + H2C C
Page 159 and 160:
Homometallic Alkoxides 157 43. J.S.
Page 161 and 162:
Homometallic Alkoxides 159 122. P.N
Page 163 and 164:
Homometallic Alkoxides 161 201. A.
Page 165 and 166:
Homometallic Alkoxides 163 281. R.C
Page 167 and 168:
Homometallic Alkoxides 165 358. L.A
Page 169 and 170:
Homometallic Alkoxides 167 430. M.R
Page 171 and 172:
Homometallic Alkoxides 169 521. I.
Page 173 and 174:
Homometallic Alkoxides 171 N.I. Koz
Page 175 and 176:
Page 177 and 178:
Page 179 and 180:
Homometallic Alkoxides 177 876. J.
Page 181 and 182:
Homometallic Alkoxides 179 966. H.
Page 183 and 184:
Homometallic Alkoxides 181 1054. M.
Page 185 and 186:
184 Alkoxo and Aryloxo Derivatives
Page 187 and 188:
Page 189 and 190:
Page 191 and 192:
Page 193 and 194:
Page 195 and 196:
Page 197 and 198:
Page 199 and 200:
Page 201 and 202:
Page 203 and 204:
Page 205 and 206:
Page 207 and 208:
Page 209 and 210:
Page 211 and 212:
Page 213 and 214:
Page 215 and 216:
Page 217 and 218:
Page 219 and 220:
Page 221 and 222:
Page 223 and 224:
Page 225 and 226:
Page 227 and 228:
Page 229 and 230:
Page 231 and 232:
Page 233 and 234:
Page 235 and 236:
Page 237 and 238:
236 Table 4.1 (Continued) M-O Bond
Page 239 and 240:
Page 241 and 242:
Page 243 and 244:
Page 245 and 246:
244 Table 4.3 Alkoxides of aluminiu
Page 247 and 248:
Page 249 and 250:
248 Table 4.4 Alkoxides of germaniu
Page 251 and 252:
Page 253 and 254:
Page 255 and 256:
Page 257 and 258:
256 Table 4.6 Alkoxides of scandium
Page 259 and 260:
Page 261 and 262:
Page 263 and 264:
Page 265 and 266:
264 Table 4.7 Alkoxides of lanthani
Page 267 and 268:
Page 269 and 270:
Page 271 and 272:
270 Table 4.8 (Continued) M-O Bond
Page 273 and 274:
Page 275 and 276:
Page 277 and 278: 276 Table 4.9 Alkoxides of titanium
Page 279 and 280: 278 Table 4.9 (Continued) Bond leng
Page 281 and 282: 280 Alkoxo and Aryloxo Derivatives
Page 301 and 302: 300 Table 4.11 Alkoxides of chromiu
Page 303 and 304: 302 Table 4.11 (Continued) Metal M-
Page 305 and 306: 304 Table 4.11 (Continued) M-O Bond
Page 317 and 318: 316 Table 4.11 (Continued) Metal M-
Page 323 and 324: 322 Table 4.12 Alkoxides of mangane
Page 327: 326 Alkoxo and Aryloxo Derivatives
Page 333 and 334: 332 Table 4.16 Alkoxides of zinc, c
Page 341 and 342: 340 Table 4.17 (Continued) Coordina
Page 349 and 350: 348 Table 4.18 Bimetallic alkoxides
Page 355 and 356: 354 Table 4.19 Heterometallic alkox
Page 379 and 380:
Page 381 and 382:
Page 383 and 384:
Page 385 and 386:
Page 387 and 388:
Page 389 and 390:
Page 391 and 392:
Page 393 and 394:
Page 395 and 396:
394 Table 5.2 Chemical shifts from
Page 397 and 398:
Page 399 and 400:
Page 401 and 402:
400 Table 5.3 Scandium, yttrium, la
Page 403 and 404:
402 Table 5.3 (continued) Metal Oxo
Page 405 and 406:
Page 407 and 408:
406 Table 5.4 Titanium and zirconiu
Page 409 and 410:
Page 411 and 412:
Page 413 and 414:
Page 415 and 416:
Page 417 and 418:
Page 419 and 420:
Page 421 and 422:
420 Table 5.6 Chromium sub-group me
Page 423 and 424:
Page 425 and 426:
Page 427 and 428:
Page 429 and 430:
Page 431 and 432:
Page 433 and 434:
Page 435 and 436:
Page 437 and 438:
Page 439 and 440:
Page 441 and 442:
Page 443 and 444:
Page 445 and 446:
1 INTRODUCTION 6 Metal Aryloxides T
Page 447 and 448:
Metal Aryloxides 447 or both of the
Page 449 and 450:
R1 OH O R2 R3NH2 −H2O Scheme 6.3
Page 451 and 452:
Cl S N N OH O Cl Me 3C NH HN OH HO
Page 453 and 454:
N OH N OH Me 3C Me3C HO HO N N OH H
Page 455 and 456:
Metal Aryloxides 455 2Ln C 3Hg⊲C6
Page 457 and 458:
Metal Aryloxides 457 Mixed halo, ar
Page 459 and 460:
product metal aryloxide 1e,1f (Eqs
Page 461 and 462:
Metal Aryloxides 461 Eqs 6.39 and 6
Page 463 and 464:
O Mg Mg OAr O Metal Aryloxides 463
Page 465 and 466:
3.7 From Metal Hydrides Metal Arylo
Page 467 and 468:
Metal Aryloxides 467 Two other impo
Page 469 and 470:
Metal Aryloxides 469 Table 6.1 Meta
Page 471 and 472:
Table 6.3 W-OAr distances for vario
Page 473 and 474:
Metal Aryloxides 473 At first it is
Page 475 and 476:
Zr−O distance (Å) V−O distance
Page 477 and 478:
Metal Aryloxides 477 as expected ar
Page 479 and 480:
Metal Aryloxides 479 whereas R D Me
Page 481 and 482:
where OAr = O But But H3C H3C O Ta
Page 483 and 484:
PPh 2 Ph P Pt OAr PPh2 where OAr =
Page 485 and 486:
6 SURVEY OF METAL ARYLOXIDES 6.1 Sp
Page 487 and 488:
487 Na2[V(O) 2(OAr) 2]2.4H2O.DMF 6-
Page 489 and 490:
489 [Tc(O)(OAr)(di-OAr)] 8-quin 2.0
Page 491 and 492:
491 [Ni3⊲OAr⊳6][ClO4].EtOH 8-qu
Page 493 and 494:
493 [Pt(OAr⊳2](tcnq) sq. planar P
Page 495 and 496:
495 [Al(OAr) 3].MeOH 8-quin 1.850 (
Page 497 and 498:
497 [Sb(OAr) 2⊲S2COEt⊳] pentago
Page 499 and 500:
499 [Tc(O)(OAr)(N-salicylideneDD-gl
Page 501 and 502:
Metal Aryloxides 501 A contribution
Page 503 and 504:
503 Table 6.8 Metal bi-phenolates B
Page 505 and 506:
505 Table 6.9 Metal binaphtholates
Page 507 and 508:
507 [TiCl2(di-OAr)]2 two tetrahedra
Page 509 and 510:
Metal Aryloxides 509 co-workers hav
Page 511 and 512:
511 [Li⊲ 2-OAr⊳]3 planar Li3O3
Page 513 and 514:
513 Table 6.11 Sodium aryloxides Bo
Page 515 and 516:
Table 6.12 Potassium aryloxides Met
Page 517 and 518:
Table 6.15 Magnesium aryloxides Met
Page 519 and 520:
519 Table 6.18 Barium aryloxides Bo
Page 521 and 522:
521 Table 6.19 Group 3 metal and la
Page 523 and 524:
523 [Me4N]La2Na2⊲ 4-OAr⊳⊲ 3-O
Page 525 and 526:
525 [Nd⊲OC6H3Ph- 6-C6H5⊳⊲OC6H
Page 527 and 528:
527 [⊲THF⊳Li⊲ 2-OAr⊳2Sm⊲C
Page 529 and 530:
529 [Eu⊲ 2-OAr⊳4⊲OAr⊳2⊲ 3
Page 531 and 532:
531 [Yb(OAr) 3⊲THF⊳2].THF squar
Page 533 and 534:
Metal Aryloxides 533 carbon atoms a
Page 535 and 536:
535 [Cp Ł Th(OAr)⊲CH2SiMe3⊳2]
Page 537 and 538:
Metal Aryloxides 537 amido compound
Page 539 and 540:
539 Table 6.21 Titanium aryloxides
Page 541 and 542:
541 [Ti2⊲ 2-OAr⊳2(OAr) 2Cl4]2 e
Page 543 and 544:
543 [Ti(OAr) 2⊲NMe2⊳2] tetrahed
Page 545 and 546:
545 [Ti(OAr) 3Bu t ] tetrahedral Ti
Page 547 and 548:
547 [⊲ArO⊳2Ti⊲ 2-ButNDCC4Et4C
Page 549 and 550:
549 [Cp⊲C5H3Me-Pri-1,2)Ti(OAr)Cl]
Page 551 and 552:
551 [CpTi(OAr) 2⊲HPPh⊳] OC6H3Pr
Page 553 and 554:
553 [Ti⊲di-OAr⊳Cl2].THF 6-coord
Page 555 and 556:
555 Table 6.22 Zirconium aryloxides
Page 557 and 558:
557 [Zr(Ind-OAr) 2] 1-indenylphenox
Page 559 and 560:
559 [Cp2Zr(OAr)] 18-electron Zr, tw
Page 561 and 562:
Metal Aryloxides 561 The thermal st
Page 563 and 564:
Metal Aryloxides 563 can only arise
Page 565 and 566:
565 1.839 (2) 138 1.854 (2) 140 [(t
Page 567 and 568:
567 [V(OAr) 3-N-Li(THF) 3] tetrahed
Page 569 and 570:
569 [V(O)(di-OAr)] 6-coord. V, both
Page 571 and 572:
571 cis,mer-[Nb(OAr) 2Cl3(THF)] dis
Page 573 and 574:
573 [Nb⊲OC6H3Ph- 4-C6H7⊳⊲OAr
Page 575 and 576:
575 Table 6.26 Tantalum aryloxides
Page 577 and 578:
577 [(THF)(ArO) 3Ta⊲DNND⊳Ta(OAr
Page 579 and 580:
579 [Ta(OAr) 2Cl2⊲CH2C6H5⊳] tbp
Page 581 and 582:
581 [Ta(OAr) 2Cl⊲ 6-C6Me6⊳] OC6
Page 583 and 584:
583 [Ta(OAr)⊲OC6H3Pri- 2-CMeDCH2
Page 585 and 586:
585 [f(TMEDA)Na⊲ 2-OAr⊳2g2Cr] 4
Page 587 and 588:
587 Table 6.28 Molybdenum aryloxide
Page 589 and 590:
589 [Mo2⊲OAr⊳5⊲NMe2⊳⊲HNMe
Page 591 and 592:
591 [Mo(Hdi-OAr) 2] 6-coord. Mo, on
Page 593 and 594:
593 [W2⊲OAr⊳6⊲HNMe2⊳2] OC6F
Page 595 and 596:
595 [W(OAr) 2⊲DNBu t ⊳2] OC6H3P
Page 597 and 598:
597 [W(OC6H3Ph- 1-C6H4⊳2⊲PMePh2
Page 599 and 600:
599 [W⊲OC6HPh3- 1-C6H4-c-C5H8C- O
Page 601 and 602:
601 [⊲OC⊳3Mn⊲C4H4N⊳Mn⊲CO3
Page 603 and 604:
603 Table 6.32 Simple aryloxides of
Page 605 and 606:
Page 607 and 608:
607 [NEt4]3fFe6⊲ 4-S⊳4⊲OAr⊳
Page 609 and 610:
609 [Ru(OAr) 2(CO)(py-CMeO-4)] cis-
Page 611 and 612:
Table 6.35 Simple aryloxides of osm
Page 613 and 614:
Metal Aryloxides 613 states, e.g. [
Page 615 and 616:
Bu t O Bu t (6-I) Bu t Bu t O Metal
Page 617 and 618:
6.2.10 Group 9 Metal Aryloxides Met
Page 619 and 620:
Table 6.38 Simple aryloxides of iri
Page 621 and 622:
Metal Aryloxides 621 Table 6.39 (Co
Page 623 and 624:
623 [Pd(OAr)⊲C6H3fCH2NMe2g2-2,6)]
Page 625 and 626:
Metal Aryloxides 625 Table 6.41 Sim
Page 627 and 628:
Page 629 and 630:
629 [(RNC) 2Cu⊲ 2-OAr⊳2Cu(CNR)
Page 631 and 632:
Metal Aryloxides 631 The two-coordi
Page 633 and 634:
Table 6.45 (Continued) Metal Arylox
Page 635 and 636:
Table 6.47 Simple aryloxides of mer
Page 637 and 638:
637 Table 6.48 Aluminium aryloxides
Page 639 and 640:
639 [⊲ArO⊳2Al⊲ -OAr⊳2Mg(THF
Page 641 and 642:
641 [Al(OAr) 2⊲i-Bu⊳] trigonal
Page 643 and 644:
643 [Al(OAr)Cl(Me)⊲NH2But⊳] OC6
Page 645 and 646:
645 Table 6.49 Gallium aryloxides B
Page 647 and 648:
647 Table 6.50 Indium aryloxides Bo
Page 649 and 650:
Metal Aryloxides 649 Table 6.53 Tin
Page 651 and 652:
651 Table 6.56 Bismuth aryloxides B
Page 653 and 654:
REFERENCES Metal Aryloxides 653 1.
Page 655 and 656:
Metal Aryloxides 655 56. Y. Nakayam
Page 657 and 658:
Metal Aryloxides 657 123. T.W. Coff
Page 659 and 660:
Metal Aryloxides 659 202. A. Bell,
Page 661 and 662:
Metal Aryloxides 661 268. K. Ishiha
Page 663 and 664:
Metal Aryloxides 663 341. B.S. Kali
Page 665 and 666:
Metal Aryloxides 665 405. P.N. Rile
Page 667 and 668:
Metal Aryloxides 667 483. Y. Hayash
Page 669 and 670:
Metal Aryloxides 669 561. A.P. Shre
Page 671 and 672:
Page 673 and 674:
Page 675 and 676:
Page 677 and 678:
Page 679 and 680:
Page 681 and 682:
Page 683 and 684:
Page 685 and 686:
Page 687 and 688:
688 Index alkoxometallate(IV) ligan
Page 689 and 690:
690 Index cerium oxo-isopropoxide 3
Page 691 and 692:
692 Index gas-phase photoelectron s
Page 693 and 694:
694 Index lead tert-butoxide 386 Le
Page 695 and 696:
696 Index metal-hydrogen bonds clea
Page 697 and 698:
698 Index oxo-alkoxides 384, 385, 3
Page 699 and 700:
700 Index sodium hydroxide 142 sodi
Page 701 and 702:
702 Index titanium dichloride dieth
Page 703:
704 Index X X-ray Absorption Near E
show all

2 Homometallic Alkoxides

Create successful ePaper yourself

Delete template?

Save as template?