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Spectrochemical series

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259:
orbitals are potentially π donors. These types of ligands tend to donate these electrons to the metal along with the σ bonding electrons, exhibiting stronger metal-ligand interactions and an effective decrease of Δ. Most halide ligands as well as OH are primary examples of π donor ligands.
385: 244:, are σ bond donors only, with no orbitals of appropriate symmetry for π bonding interactions. Bonding by these ligands to metals is relatively simple, using only the σ bonds to create relatively weak interactions. Another example of a σ bonding ligand would be 224:
Ligands arranged on the left end of this spectrochemical series are generally regarded as weaker ligands and cannot cause forcible pairing of electrons within the 3d level, and thus form outer orbital octahedral complexes that are
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In general, it is not possible to say whether a given ligand will exert a strong field or a weak field on a given metal ion. However, when we consider the metal ion, the following two useful trends are observed:
229:. On the other hand, ligands lying at the right end are stronger ligands and form inner orbital octahedral complexes after forcible pairing of electrons within 3d level and hence are called low spin ligands. 232:
However, it is known that "the spectrochemical series is essentially backwards from what it should be for a reasonable prediction based on the assumptions of crystal field theory." This deviation from
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The order of the spectrochemical series can be derived from the understanding that ligands are frequently classified by their donor or acceptor abilities. Some, like NH
271:, and the ligands may be π acceptors. This addition to the bonding scheme increases Δ. Ligands that do this very effectively include CN, CO, and many others. 450: 431: 71:
The spectrochemical series was first proposed in 1938 based on the results of absorption spectra of cobalt complexes.
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can also be arranged in order of increasing Δ, and this order is largely independent of the identity of the ligand.
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highlights the weakness of crystal field theory's assumption of purely ionic bonds between metal and ligand.
470: 226: 60: 309: 234: 52: 8: 410: 44: 193: 174: 427: 365: 56: 28: 31:, group and element. For a metal ion, the ligands modify the difference in energy 326:
Fifth Edition. Boston: Houghton Mifflin Company, 2005. Pages 550-551 and 957-964.
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listing of ligands from small Δ to large Δ is given below. (For a table, see the
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has a stronger effect than ammonia, generating a larger ligand field split, Δ.
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List of ligands in coordination compounds topic of Inorganic chemistry
124: 36: 63:, and optical properties such as its color and absorption spectrum. 340:
4th edition, HarperCollins College Publishers, 1993. Pages 405-408.
159: 120: 102: 55:. The splitting parameter is reflected in the ion's electronic and 197: 182: 106: 94: 90: 287:
Mn < Ni < Co < Fe < V < Fe < Cr < V < Co
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ordered by ligand "strength", and a list of metal ions based on
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Inorganic Chemistry: Principles of Structure and Reactivity
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3rd edition, Oxford University Press, 2001. Pages: 227-236.
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orbitals of suitable energy, there is the possibility of
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James E. Huheey, Ellen A. Keiter, and Richard L. Keiter
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http://science.marshall.edu/castella/chm448/chap11.pdf
66: 355:"Absorption Spectra of Co-ordination Compounds. I." 274: 312: – Term in the chemistry of transition metals 426:(4th ed.). Prentice Hall. pp. 395–396. 296:Δ increases with increasing oxidation number, and 462: 451:"The Spectrochemical Series – Every Science" 421: 352: 369: 463: 445: 443: 422:Miessler, Gary; Tarr, Donald (2011). 13: 440: 14: 487: 67:Spectrochemical series of ligands 49:crystal-field splitting parameter 275:Spectrochemical series of metals 263:When ligands have vacant π* and 214:Strong field ligands: CO, CN, NH 41:ligand-field splitting parameter 329:D. F. Shriver and P. W. Atkins 415: 403: 378: 346: 1: 386:"B.2. Spectrochemical Series" 316: 7: 303: 255:Ligands that have occupied 10: 492: 299:Δ increases down a group. 476:Coordination chemistry 76:spectrochemical series 21:spectrochemical series 207:Weak field ligands: H 390:Chemistry LibreTexts 358:Bull. Chem. Soc. Jpn 353:R. Tsuchida (1938). 310:Nephelauxetic effect 235:crystal field theory 53:crystal field theory 471:Inorganic chemistry 424:Inorganic Chemistry 371:10.1246/bcsj.13.388 331:Inorganic Chemistry 324:Chemical Principles 322:Zumdahl, Steven S. 188:(N–bonded) < PPh 57:magnetic properties 45:ligand field theory 194:Triphenylphosphine 177:) < phen (1,10- 433:978-0-13-612866-3 483: 455: 454: 447: 438: 437: 419: 413: 407: 401: 400: 398: 397: 382: 376: 375: 373: 350: 150:(N–bonded) < 101:(S–bonded) < 29:oxidation number 491: 490: 486: 485: 484: 482: 481: 480: 461: 460: 459: 458: 449: 448: 441: 434: 420: 416: 408: 404: 395: 393: 384: 383: 379: 351: 347: 319: 306: 277: 250:ethylenediamine 246:ethylenediamine 243: 221: 217: 210: 191: 186: 175:2,2'-bipyridine 171:ethylenediamine 167: 155: 143: 136: 132: 117: 110: 69: 17: 12: 11: 5: 489: 479: 478: 473: 457: 456: 439: 432: 414: 402: 377: 364:(5): 388–400. 344: 343: 342: 341: 334: 327: 318: 315: 314: 313: 305: 302: 301: 300: 297: 289: 288: 276: 273: 269:pi backbonding 241: 219: 215: 208: 205: 204: 189: 184: 179:phenanthroline 173:) < bipy ( 165: 153: 141: 134: 130: 115: 108: 68: 65: 15: 9: 6: 4: 3: 2: 488: 477: 474: 472: 469: 468: 466: 452: 446: 444: 435: 429: 425: 418: 412: 406: 391: 387: 381: 372: 367: 363: 359: 356: 349: 345: 339: 335: 332: 328: 325: 321: 320: 311: 308: 307: 298: 295: 294: 293: 286: 285: 284: 282: 272: 270: 266: 261: 258: 253: 251: 247: 238: 236: 230: 228: 222: 212: 211:O, F, Cl, OH 203: 199: 195: 187: 180: 176: 172: 168: 161: 157: 149: 145: 137: 126: 122: 118: 111: 104: 100: 96: 92: 88: 85: 84: 83: 81: 77: 72: 64: 62: 58: 54: 50: 46: 42: 39:, called the 38: 34: 30: 26: 23:is a list of 22: 423: 417: 409:7th page of 405: 394:. Retrieved 392:. 2016-09-05 389: 380: 361: 357: 348: 337: 330: 323: 290: 278: 264: 262: 256: 254: 239: 231: 223: 213: 206: 75: 73: 70: 59:such as its 48: 40: 35:between the 32: 20: 18: 248:; however, 465:Categories 396:2023-03-05 317:References 281:metal ions 74:A partial 61:spin state 37:d orbitals 227:high spin 169:< en ( 158:< py ( 47:, or the 304:See also 160:pyridine 196:) < 181:) < 162:) < 82:page.) 25:ligands 430:  80:ligand 218:, PPh 200:< 146:< 138:< 127:< 123:< 119:< 112:< 105:< 97:< 93:< 89:< 428:ISBN 279:The 366:doi 148:NCS 99:SCN 51:in 43:in 467:: 442:^ 388:. 362:13 360:. 202:CO 198:CN 183:NO 164:NH 156:CN 152:CH 125:OH 107:NO 103:Cl 91:Br 19:A 453:. 436:. 399:. 374:. 368:: 265:d 257:p 242:3 220:3 216:3 209:2 192:( 190:3 185:2 166:3 154:3 144:O 142:2 140:H 135:4 133:O 131:2 129:C 121:F 116:3 114:N 109:3 95:S 87:I 33:Δ

Index

ligands
oxidation number
d orbitals
ligand field theory
crystal field theory
magnetic properties
spin state
ligand
I
Br
S
SCN
Cl
NO3
N3
F
OH
C2O4
H2O
NCS
CH3CN
pyridine
NH3
ethylenediamine
2,2'-bipyridine
phenanthroline
NO2
Triphenylphosphine
CN
CO

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