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Palladium(II) acetate

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66: 57: 307: 198: 35: 549: 554: 544: 44: 1135: 689: 880:. Likewise, palladium(II) acetate can be prepared by treating other palladium(II) carboxylates with acetic acid. This ligand exchange starting with a purified other carboxylate is an alternative way to synthesize palladium(II) acetate free from the nitro contaminant. 868:
Relative to the trimeric acetate, the mixed nitrate-acetate variant has different solubility and catalytic activity. Preventing, or controlling for the amount of, this impurity can be an important aspect for reliable use of palladium(II) acetate.
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Basu, B., Satadru J., Mosharef H. B., and Pralay D. (2003). "A Simple Protocol for the Direct Reductive Amination of Aldehydes and Ketones Using Potassium Formate and Catalytic Palladium Acetate".
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as monoclinic plates. It has a trimeric structure, consisting of an equilateral triangle of Pd atoms each pair of which is bridged with two acetate groups in a butterfly conformation.
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Herrmann, W. A.; Brossmer, C.; Reisinger, C.-P.; Riermeier, T. H.; Öfele, K.; Beller, M. (1997). "Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl Halides".
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Herrmann, W. A.; Brossmer, C.; Reisinger, C.-P.; Riermeier, T. H.; Öfele, K.; Beller, M. (1997). "Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl Halides".
702: 1554: 756:, the compound exists as molecular and polymeric forms with the trimeric form being the dominant form in the solid state and in solution. Pd achieves approximate 1738: 767:
and coworkers in 1965 and later characterized by Skapski and Smart in 1970 by single crystal X-ray diffraction, palladium(II) acetate is a red-brown solid that
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is compatible with the electronic properties of aryl bromides, and unlike other methods of synthesis, this method does not require high pressure equipment.
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Nikitin, Kirill V.; Andryukhova, N.P.; Bumagin, N.A.; Beletskaya, I.P. (1991). "Synthesis of Aryl Esters by Pd-catalysed Carbonylation of Aryl Iodides".
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Palladium acetate is used to produce other palladium(II) compounds. For example, phenylpalladium acetate, used to isomerize allyl alcohols to
1224: 1383: 744:. Depending on the value of n, the compound is soluble in many organic solvents and is commonly used as a catalyst for organic reactions. 147: 1439:
Suggs, J W. "Palladium: Organometallic Chemistry." Encyclopedia of Inorganic Chemistry. Ed. R B. King. 8 vols. Chichester: Wiley, 1994.
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Bakhmutov, V. I.; Berry, J. F.; Cotton, F. A.; Ibragimov, S.; Murillo, C. A. (2005). "Non-Trivial Behavior of Palladium(II) Acetate".
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Palladium(II) acetate can also be prepared as a pale pink form. According to X-ray powder diffraction, this form is polymeric.
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Grennberg, Helena; Foot, Jonathan S.; Banwell, Martin G.; Roman, Daniela Sustac (2001). "Palladium(II) Acetate".
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Keary M. Engle; Navid Dastbaravardeh; Peter S. Thuy-Boun; Dong-Hui Wang; Aaron C. Sather; Jin-Quan Yu (2015).
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Linli He; Shawn P. Allwein; Benjamin J. Dugan; Kyle W. Knouse; Gregory R. Ott; Craig A. Zificsak (2016).
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Palladium acetate, in trimeric form, can be prepared by treating palladium sponge with a mixture of
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Palladium(II) acetate is prone to reduction to Pd(0) in the presence of reagents which can undergo
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Skapski, A C.; M. L. Smart (1970). "The Crystal Structure of Trimeric Palladium(II) Acetate".
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Ritter, Stephen K. (May 2, 2016). "Chemists introduce a user's guide for palladium acetate".
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or nitrogen gas flow are required to prevent contamination by the mixed nitrito-acetate (Pd
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Gooben, L J. "Research Area "New Pd-Catalyzed Cross-Coupling Reactions"" 28 Feb. 2006<
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Light or heat reduce palladium acetate to give thin layers of palladium and can produce
3011: 2693: 2633: 2620: 2521: 2293: 2274: 1475: 1450: 964: 680: 3066: 2667: 2260: 1105: 944: 932: 431: 186: 1511: 1249:(1965). "667. Carboxylates of palladium, platinum, and rhodium, and their adducts". 2491: 972: 918: 791: 768: 582: 237: 1216: 992:, a functional group in many organic compounds including the fungicide "Latitude". 369:
coordination form (cyclic trimer): O0(C)O3(O(C)O1)O(C)O1(O(C)O2)O(C)O02O(C)O3
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Palladium acetate is a catalyst for many organic reactions, especially
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http://www.mpi-muelheim.mpg.de/kofo/bericht2002/pdf/2.1.8_gossen.pdf
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are prepared by treating palladium(II) acetate with the appropriate
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Except where otherwise noted, data are given for materials in their
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reactions: for example, the formation of esters from aryl iodides,
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T. A. Stephenson; S. M. Morehouse; A. R. Powell; J. P. Heffer;
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With a 1:2 stoichiometric ratio of palladium atoms and acetate
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InChI=1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
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Palladium(II) propionate is prepared analogously; other
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InChI=1/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
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Kirik, S.D.; Mulagaleev, S.F.; Blokhin, A.I. (2004). "
2114: 2095: 2072: 2022: 1833: 1785: 1754: 1406: 1404: 938:Rearrangement of acyclic dienes: An example is the 1121:is made by reaction of palladium(II) acetate with 887:such as primary and secondary alcohols as well as 436:205 °C (401 °F; 478 K) decomposes 236: 121: 1209:Encyclopedia of Reagents for Organic Synthesis 924:Reactions catalyzed by palladium(II) acetate: 2166: 1732: 8: 1553:: CS1 maint: multiple names: authors list ( 1240: 1238: 1236: 1334: 1332: 2173: 2159: 2151: 2019: 1782: 1739: 1725: 1717: 1602:"Buchwald-Hartwig Cross Coupling Reaction" 305: 196: 174: 26: 1585: 1474: 1251:Journal of the Chemical Society (Resumed) 1071:, is prepared by the following reaction: 985:/pseudohalides with alkyl an aryl amines. 272: 1097: 1093: 1089: 1085: 1081: 1077: 1039: 1035: 1031: 1027: 1023: 1019: 1015: 1011: 1007: 1003: 999: 861: 857: 853: 849: 845: 841: 837: 828: 824: 820: 816: 812: 153:coordination form (cyclic trimer): 1177: 361: 326: 301: 2203: 1546: 905:Palladium-catalyzed coupling reactions 187: 2869: 1299:from X-ray Powder Diffraction Data". 988:conversion of aryl bromides into the 333:Key: YJVFFLUZDVXJQI-UHFFFAOYSA-L 7: 2193: 343:Key: YJVFFLUZDVXJQI-NUQVWONBAH 227: 1373:"High Purity Homogeneous Catalyst" 1104:Palladium(II) acetate reacts with 975:(precursor to poly(vinyl acetate). 25: 2181:Acetyl halides and salts of the 1382:. September 2005. Archived from 687: 552: 547: 542: 42: 33: 1512:10.1070/MC1991v001n04ABEH000080 1414:Chemical & Engineering News 1108:(the "acac" ligand) to produce 1063:Precursor to other Pd compounds 742:the analogous platinum compound 683:(at 25 °C , 100 kPa). 364:ionic form: .C(=O)C.C(=O)C 1695:Chemistry – A European Journal 1668:Chemistry – A European Journal 506:Occupational safety and health 1: 2023:Organopalladium(II) compounds 1217:10.1002/047084289X.rp001.pub3 1186:"520764 [Pd(OAc)2]3" 740:. It is more reactive than 98:hexakis(acetato)tripalladium 1604:. Organic Chemistry Portal. 51: 3094: 2871: 1654:, vol. 6, p. 815 1570:"Synthesis of α-Carboline" 1427:10.1021/cen-09418-scitech1 979:Buchwald-Hartwig amination 921:to form reactive adducts. 902: 758:square planar coordination 408:224.51 g/mol 2205: 2190: 1315:10.1107/S0108270104016129 790:. An excess of palladium 732:described by the formula 677: 642: 523: 503: 498: 452: 377: 352: 317: 105: 93: 83: 78: 50: 41: 32: 1707:10.1002/chem.19970030823 1680:10.1002/chem.19970030823 1587:10.15227/orgsyn.093.0272 1500:Mendeleev Communications 1467:10.15227/orgsyn.092.0058 885:beta-hydride elimination 599:Precautionary statements 519:considered nonhazardous 951:, an alcohol or phenol. 917:, and alkyl, aryl, and 1622:July 12, 2007, at the 1541:10.1002/chin.200330069 1143: 935:and related processes. 657:Palladium(II) chloride 69: 60: 28:Palladium(II) acetate 1166:Saegusa–Ito oxidation 1137: 961:by potassium formate. 722:Palladium(II) acetate 474:Coordination geometry 100:bis(acetato)palladium 88:Palladium(II) acetate 68: 59: 1282:10.1039/C2970000658b 1259:10.1039/jr9650003632 931:: An example is the 672:Platinum(II) acetate 3073:Palladium compounds 1748:Palladium compounds 1342:Dalton Transactions 1302:Acta Crystallogr. C 1140:Herrmann's catalyst 1119:Herrmann's catalyst 967:: the oxidation of 955:Reductive amination 443:Solubility in water 416:Brown yellow solid 96:Palladium diacetate 29: 1144: 940:Cope rearrangement 765:Geoffrey Wilkinson 710:Infobox references 643:Related compounds 70: 61: 27: 3060: 3059: 3054: 3053: 2148: 2147: 2068: 2067: 1829: 1828: 1652:Collected Volumes 1645:Organic Syntheses 1345:(11): 1989–1992. 1226:978-0-470-84289-8 1211:. pp. 1–35. 726:chemical compound 718:Chemical compound 716: 715: 632:Safety data sheet 577:Hazard statements 460:Crystal structure 286:CompTox Dashboard 156:Interactive image 148:Interactive image 145:ionic form: 74: 73: 18:Palladium acetate 16:(Redirected from 3085: 2194: 2175: 2168: 2161: 2152: 2020: 1783: 1741: 1734: 1727: 1718: 1711: 1710: 1701:(8): 1357–1364. 1690: 1684: 1683: 1663: 1657: 1655: 1648: 1632: 1626: 1612: 1606: 1605: 1598: 1592: 1591: 1589: 1565: 1559: 1558: 1552: 1544: 1522: 1516: 1515: 1495: 1489: 1488: 1478: 1446: 1440: 1437: 1431: 1430: 1408: 1399: 1398: 1396: 1394: 1389:on 17 March 2006 1388: 1377: 1369: 1363: 1362: 1351:10.1039/b502122g 1336: 1327: 1326: 1309:(9): m449–m450. 1292: 1286: 1285: 1276:(11): 658b–659. 1269: 1263: 1262: 1242: 1231: 1230: 1204: 1198: 1197: 1195: 1193: 1182: 1127:-tolyl)phosphine 1100: 1096:)(OAc) + Hg(OAc) 1084:)(OAc) + Pd(OAc) 1043: 990:trimethylsilanes 957:of aldehydes or 864: 832: 700: 694: 691: 690: 626: 622: 618: 614: 610: 606: 592: 588: 584: 556: 551: 546: 385:Chemical formula 310: 309: 294: 292: 276: 240: 229: 208: 200: 189: 178: 158: 150: 125: 52: 46: 37: 30: 21: 3093: 3092: 3088: 3087: 3086: 3084: 3083: 3082: 3063: 3062: 3061: 3056: 3055: 3019: 3015: 3004: 2996: 2983: 2975: 2967: 2959: 2951: 2943: 2935: 2927: 2919: 2908: 2900: 2892: 2884: 2796: 2788: 2783: 2781: 2773: 2768: 2761: 2756: 2754: 2750: 2742: 2734: 2708: 2697: 2679: 2674: 2670: 2660: 2652: 2647: 2645: 2637: 2629: 2616: 2608: 2604: 2596: 2591: 2588: 2584: 2573: 2562: 2554: 2544: 2524: 2514: 2503: 2495: 2487: 2482: 2475: 2467: 2459: 2454: 2452: 2444: 2439: 2437: 2429: 2424: 2422: 2414: 2406: 2398: 2388: 2368: 2352: 2348: 2344: 2339: 2336: 2331: 2328: 2323: 2319: 2317: 2309: 2301: 2296: 2282: 2269: 2259: 2252: 2248: 2243: 2241: 2233: 2229: 2224: 2222: 2186: 2179: 2149: 2144: 2140: 2126: 2110: 2106: 2091: 2087: 2083: 2064: 2060: 2056: 2052: 2048: 2040: 2036: 2032: 2018: 2014: 2010: 2006: 2002: 1998: 1990: 1986: 1982: 1978: 1974: 1970: 1966: 1958: 1954: 1946: 1928: 1924: 1916: 1912: 1904: 1896: 1888: 1880: 1872: 1864: 1860: 1856: 1848: 1844: 1825: 1822: 1818: 1814: 1810: 1806: 1802: 1798: 1787:Organopalladium 1781: 1777: 1773: 1769: 1765: 1750: 1745: 1715: 1714: 1692: 1691: 1687: 1665: 1664: 1660: 1650: 1636:Richard F. Heck 1634: 1633: 1629: 1624:Wayback Machine 1613: 1609: 1600: 1599: 1595: 1567: 1566: 1562: 1545: 1535:(30): 555–557. 1524: 1523: 1519: 1497: 1496: 1492: 1448: 1447: 1443: 1438: 1434: 1410: 1409: 1402: 1392: 1390: 1386: 1375: 1371: 1370: 1366: 1338: 1337: 1330: 1298: 1294: 1293: 1289: 1274:J. Chem. Soc. D 1271: 1270: 1266: 1244: 1243: 1234: 1227: 1206: 1205: 1201: 1191: 1189: 1188:. Sigma-Aldrich 1184: 1183: 1179: 1174: 1162: 1113: 1099: 1095: 1091: 1087: 1083: 1079: 1075: 1065: 1058: 1054: 1050: 1041: 1037: 1033: 1029: 1025: 1021: 1017: 1013: 1009: 1005: 1001: 997: 949:carbon monoxide 907: 901: 878:carboxylic acid 863: 859: 855: 851: 847: 843: 839: 835: 830: 826: 822: 818: 814: 810: 805: 801: 797: 780: 763:As prepared by 760:in both forms. 750: 739: 735: 719: 712: 707: 706: 705:  ?) 696: 692: 688: 684: 668: 653: 601: 579: 565: 539: 516: 488: 476: 462: 445: 397: 393: 387: 373: 370: 365: 360: 359: 348: 345: 344: 341: 335: 334: 331: 325: 324: 313: 295: 288: 279: 259: 243: 230: 218: 181: 161: 139: 128: 115: 101: 99: 97: 89: 23: 22: 15: 12: 11: 5: 3091: 3089: 3081: 3080: 3075: 3065: 3064: 3058: 3057: 3052: 3051: 3048: 3045: 3042: 3039: 3036: 3033: 3030: 3027: 3024: 3021: 3017: 3013: 3009: 3006: 3002: 2998: 2994: 2990: 2986: 2985: 2981: 2977: 2973: 2969: 2965: 2961: 2957: 2953: 2949: 2945: 2941: 2937: 2933: 2929: 2925: 2921: 2917: 2913: 2910: 2906: 2902: 2898: 2894: 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1064: 1061: 1056: 1052: 1048: 1045: 1044: 994: 993: 986: 976: 965:Wacker process 962: 952: 942: 936: 900: 897: 895:to palladium. 866: 865: 833: 803: 799: 795: 779: 776: 749: 746: 737: 736:, abbreviated 733: 717: 714: 713: 708: 686: 685: 681:standard state 678: 675: 674: 669: 663: 660: 659: 654: 648: 645: 644: 640: 639: 635: 628: 627: 625:P305+P351+P338 602: 597: 594: 593: 580: 575: 572: 571: 566: 561: 558: 557: 540: 535: 532: 531: 521: 520: 517: 514: 511: 510: 501: 500: 496: 495: 489: 484: 481: 480: 479:square planar 477: 472: 469: 468: 463: 458: 455: 454: 450: 449: 446: 441: 438: 437: 434: 428: 427: 424: 418: 417: 414: 410: 409: 406: 400: 399: 395: 391: 388: 383: 380: 379: 375: 374: 372: 371: 368: 366: 363: 355: 354: 353: 350: 349: 347: 346: 342: 339: 338: 336: 332: 329: 328: 320: 319: 318: 315: 314: 312: 311: 303:DTXSID10890575 298: 296: 284: 281: 280: 278: 277: 269: 267: 261: 260: 258: 257: 253: 251: 245: 244: 242: 241: 233: 231: 223: 220: 219: 217: 216: 212: 210: 202: 201: 191: 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1836: 1832: 1823: 1793: 1791: 1789:(0) compounds 1788: 1784: 1778: 1760: 1759: 1757: 1753: 1749: 1742: 1737: 1735: 1730: 1728: 1723: 1722: 1719: 1708: 1704: 1700: 1696: 1689: 1686: 1681: 1677: 1674:: 1357–1364. 1673: 1669: 1662: 1659: 1653: 1647: 1646: 1641: 1637: 1631: 1628: 1625: 1621: 1617: 1611: 1608: 1603: 1597: 1594: 1588: 1583: 1579: 1575: 1571: 1564: 1561: 1556: 1550: 1542: 1538: 1534: 1530: 1529: 1521: 1518: 1513: 1509: 1505: 1501: 1494: 1491: 1486: 1482: 1477: 1472: 1468: 1464: 1460: 1456: 1452: 1445: 1442: 1436: 1433: 1428: 1424: 1421:(18): 20–21. 1420: 1416: 1415: 1407: 1405: 1401: 1385: 1381: 1374: 1368: 1365: 1360: 1356: 1352: 1348: 1344: 1343: 1335: 1333: 1329: 1324: 1320: 1316: 1312: 1308: 1304: 1303: 1291: 1288: 1283: 1279: 1275: 1268: 1265: 1260: 1256: 1252: 1248: 1241: 1239: 1237: 1233: 1228: 1222: 1218: 1214: 1210: 1203: 1200: 1187: 1181: 1178: 1171: 1167: 1164: 1163: 1159: 1157: 1155: 1151: 1141: 1138:Structure of 1136: 1132: 1131: 1130: 1128: 1126: 1120: 1116: 1114: 1107: 1106:acetylacetone 1074: 1073: 1072: 1070: 1062: 1060: 996: 995: 991: 987: 984: 980: 977: 974: 970: 966: 963: 960: 956: 953: 950: 946: 945:Carbonylation 943: 941: 937: 934: 933:Heck reaction 930: 927: 926: 925: 922: 920: 919:vinyl halides 916: 912: 906: 898: 896: 894: 890: 886: 881: 879: 875: 870: 848:COOH → Pd(O 834: 809: 808: 807: 793: 789: 785: 777: 775: 772: 770: 766: 761: 759: 755: 747: 745: 743: 731: 727: 723: 711: 704: 699: 682: 676: 673: 670: 667: 662: 661: 658: 655: 652: 647: 646: 641: 638: 636: 633: 630: 629: 603: 600: 596: 595: 581: 578: 574: 573: 570: 567: 564: 560: 559: 555: 550: 545: 541: 538: 534: 533: 529: 527: 522: 518: 513: 512: 508: 507: 502: 497: 494: 490: 487: 486:Dipole moment 483: 482: 478: 475: 471: 470: 467: 464: 461: 457: 456: 451: 447: 444: 440: 439: 435: 433: 432:Melting point 430: 429: 425: 423: 420: 419: 415: 412: 411: 407: 405: 402: 401: 389: 386: 382: 381: 376: 367: 362: 358: 351: 337: 327: 323: 316: 308: 304: 300: 299: 297: 287: 283: 282: 275: 271: 270: 268: 266: 263: 262: 255: 254: 252: 250: 247: 246: 239: 235: 234: 232: 226: 222: 221: 214: 213: 211: 209: 204: 203: 199: 195: 192: 190: 188:ECHA InfoCard 185: 184: 177: 173: 172: 170: 168: 165: 164: 157: 152: 149: 144: 143: 141: 137: 132: 131: 124: 120: 119: 117: 114: 110: 109: 104: 92: 86: 82: 77: 67: 63: 58: 54: 53: 49: 45: 40: 36: 31: 19: 2612: 2131: 2130:hypothetical 2121: 1840: 1698: 1694: 1688: 1671: 1667: 1661: 1651: 1643: 1630: 1610: 1596: 1577: 1573: 1563: 1549:cite journal 1532: 1526: 1520: 1503: 1499: 1493: 1458: 1454: 1444: 1435: 1418: 1412: 1391:. Retrieved 1384:the original 1367: 1340: 1306: 1300: 1290: 1273: 1267: 1250: 1247:G. Wilkinson 1208: 1202: 1190:. Retrieved 1180: 1147: 1124: 1117: 1103: 1066: 1046: 983:aryl halides 973:acetaldehyde 971:by water to 923: 908: 882: 874:carboxylates 871: 867: 792:sponge metal 781: 773: 769:crystallizes 762: 751: 721: 720: 568: 525: 515:Main hazards 504: 249:RTECS number 106:Identifiers 94:Other names 1393:24 February 1192:23 December 788:nitric acid 784:acetic acid 778:Preparation 563:Signal word 509:(OHS/OSH): 413:Appearance 378:Properties 194:100.020.151 3067:Categories 1574:Org. Synth 1528:ChemInform 1455:Org. Synth 1172:References 929:Vinylation 903:See also: 893:decomposes 811:Pd + 4 HNO 537:Pictograms 466:monoclinic 453:Structure 426:2.19 g/cm 404:Molar mass 274:0LTG3460Y5 167:ChemSpider 134:3D model ( 113:CAS Number 85:IUPAC name 2073:Pd(II,IV) 1461:: 58–75. 1380:Engelhard 1150:nanowires 1069:aldehydes 899:Catalysis 748:Structure 730:palladium 621:P302+P352 528:labelling 256:AJ1900000 215:222-164-4 207:EC Number 123:3375-31-3 3078:Acetates 2298:NaH(OAc) 1853:Pd((COCH 1841:Pd(OCOCH 1620:Archived 1485:27397943 1359:15909048 1323:15345831 1253:: 3632. 1160:See also 1154:colloids 1110:Pd(acac) 969:ethylene 815:→ Pd(NO 499:Hazards 3001:Th(OAc) 2993:Ac(OAc) 2980:Yb(OAc) 2972:Tm(OAc) 2964:Er(OAc) 2956:Ho(OAc) 2948:Dy(OAc) 2940:Tb(OAc) 2932:Gd(OAc) 2924:Eu(OAc) 2916:Sm(OAc) 2905:Nd(OAc) 2897:Pr(OAc) 2889:Ce(OAc) 2881:La(OAc) 2872:  2793:Bi(OAc) 2785:Pb(OAc) 2778:Pb(OAc) 2770:Tl(OAc) 2758:Hg(OAc) 2739:Au(OAc) 2731:Pt(OAc) 2705:Lu(OAc) 2694:Ba(OAc) 2657:Sb(OAc) 2649:Sn(OAc) 2642:Sn(OAc) 2634:In(OAc) 2626:Cd(OAc) 2613:Pd(OAc) 2593:Ru(OAc) 2570:Mo(OAc) 2559:Zr(OAc) 2541:Sr(OAc) 2511:As(OAc) 2500:Ga(OAc) 2492:Zn(OAc) 2484:Cu(OAc) 2472:Ni(OAc) 2464:Co(OAc) 2456:Fe(OAc) 2449:Fe(OAc) 2441:Mn(OAc) 2434:Mn(OAc) 2426:Cr(OAc) 2419:Cr(OAc) 2411:VO(OAc) 2403:Ti(OAc) 2395:Sc(OAc) 2385:Ca(OAc) 2325:Al(OAc) 2314:Al(OAc) 2306:Mg(OAc) 2219:Be(OAc) 2183:acetate 2037:CHPdCl) 1580:: 272. 1476:4936495 1088:→ Pd(C 1034:+ Si(CH 1006:Br + Si 959:ketones 911:alkenes 860:+ 2 HNO 754:ligands 703:what is 701: ( 666:cations 422:Density 398: 225:PubChem 2676:I(OAc) 2551:Y(OAc) 2333:Al(OH) 2249:O(OAc) 2238:B(OAc) 2230:O(OAc) 2115:Pd(VI) 2096:Pd(IV) 1995:Pd(P(C 1921:Pd(ClO 1885:Pd(CN) 1834:Pd(II) 1762:Pd(P(C 1483:  1473:  1357:  1321:  1223:  915:dienes 889:amines 844:+ 2 CH 823:+ 2 NO 698:verify 695:  664:Other 651:anions 649:Other 634:(SDS) 569:Danger 357:SMILES 238:167845 176:146827 79:Names 3016:(OAc) 2766:TlOAc 2751:(OAc) 2689:CsOAc 2621:AgOAc 2605:(OAc) 2585:(OAc) 2536:RbOAc 2526:BrOAc 2480:CuOAc 2370:ClOAc 2349:(OAc) 2321:ALSOL 2294:NaOAc 2275:AcOOH 2257:AcOAc 2214:LiOAc 2053:)Pd(C 1909:Pd(NO 1755:Pd(0) 1618:> 1387:(PDF) 1376:(PDF) 1123:tris( 1026:Si(CH 1018:→ RC 836:Pd(NO 827:+ 2 H 798:(OAc) 724:is a 390:Pd(CH 322:InChI 136:JSmol 2672:IOAc 2522:BrAc 2380:KOAc 2366:ClAc 2284:FOAc 2261:ROAc 2198:AcOH 2137:PdAs 2029:((CH 1987:PdCl 1963:Fe(C 1955:PdCl 1943:PdSO 1877:PdCl 1869:PdBr 1555:link 1481:PMID 1395:2006 1355:PMID 1319:PMID 1221:ISBN 1194:2021 1152:and 1076:Hg(C 1047:Pd(O 786:and 617:P280 613:P273 609:P272 605:P261 591:H410 587:H318 583:H317 448:low 394:COO) 265:UNII 3050:No 3047:Md 3044:Fm 3041:Es 3038:Cf 3035:Bk 3032:Cm 3029:Am 3026:Pu 3023:Np 3008:Pa 2989:** 2912:Pm 2865:Og 2862:Ts 2859:Lv 2856:Mc 2853:Fl 2850:Nh 2847:Cn 2844:Rg 2841:Ds 2838:Mt 2835:Hs 2832:Bh 2829:Sg 2826:Db 2823:Rf 2820:Lr 2817:** 2814:Ra 2811:Fr 2806:Rn 2803:At 2800:Po 2727:Ir 2724:Os 2721:Re 2715:Ta 2712:Hf 2683:Xe 2668:IAc 2664:Te 2577:Tc 2566:Nb 2530:Kr 2518:Se 2507:Ge 2374:Ar 2356:Si 2337:OAc 2288:Ne 2280:FAc 2270:OAc 2208:He 2185:ion 2123:PdF 2103:PdF 1971:P(C 1938:PdS 1933:PdO 1901:PdI 1893:PdF 1861:CH) 1819:CO) 1799:((C 1703:doi 1676:doi 1582:doi 1537:doi 1508:doi 1471:PMC 1463:doi 1423:doi 1347:doi 1311:doi 1278:doi 1255:doi 1213:doi 1051:CCH 1010:(CH 981:of 852:CCH 806:). 728:of 526:GHS 291:EPA 228:CID 3069:: 3012:UO 2877:* 2747:Hg 2718:W 2701:* 2601:Rh 2589:Cl 2581:Ru 2362:S 2359:P 2345:SO 2341:Al 2329:OH 2266:NH 2226:Be 2080:Pd 2045:(C 2011:Cl 1951:Na 1795:Pd 1697:. 1670:. 1649:; 1642:. 1638:. 1578:93 1576:. 1572:. 1551:}} 1547:{{ 1533:34 1531:. 1502:. 1479:. 1469:. 1459:92 1457:. 1453:. 1419:94 1417:. 1403:^ 1378:. 1353:. 1331:^ 1317:. 1307:60 1305:. 1235:^ 1219:. 1156:. 1129:. 1115:. 1042:Br 998:RC 913:, 802:NO 623:, 619:, 615:, 611:, 607:, 589:, 585:, 530:: 491:0 3018:2 3014:2 3003:4 2995:3 2982:3 2974:3 2966:3 2958:3 2950:3 2942:3 2934:3 2926:3 2918:3 2907:3 2899:3 2891:3 2883:3 2795:3 2787:4 2780:2 2772:3 2760:2 2753:2 2749:2 2741:3 2733:2 2707:3 2696:2 2678:3 2659:3 2651:4 2644:2 2636:3 2628:2 2615:2 2607:4 2603:2 2595:3 2587:4 2583:2 2572:2 2561:4 2553:3 2543:2 2513:3 2502:3 2494:2 2486:2 2474:2 2466:2 2458:3 2451:2 2443:3 2436:2 2428:3 2421:2 2413:3 2405:4 2397:3 2387:2 2351:4 2347:4 2343:2 2335:2 2327:2 2316:3 2308:2 2300:2 2268:4 2251:4 2247:2 2245:B 2240:3 2232:6 2228:4 2221:2 2174:e 2167:t 2160:v 2139:2 2132:) 2128:( 2125:6 2105:4 2086:6 2084:F 2082:2 2061:) 2059:5 2057:H 2055:3 2051:5 2049:H 2047:5 2039:2 2035:2 2033:) 2031:2 2013:2 2009:2 2007:) 2005:3 2003:) 2001:5 1999:H 1997:6 1989:2 1985:2 1983:) 1981:2 1979:) 1977:5 1975:H 1973:6 1969:4 1967:H 1965:5 1957:4 1953:2 1945:4 1927:2 1925:) 1923:4 1915:2 1913:) 1911:3 1903:2 1895:2 1887:2 1879:2 1871:2 1863:2 1859:2 1857:) 1855:3 1847:2 1845:) 1843:3 1821:3 1817:2 1815:) 1813:2 1811:H 1809:2 1807:C 1805:5 1803:H 1801:6 1797:2 1776:4 1774:) 1772:3 1770:) 1768:5 1766:H 1764:6 1740:e 1733:t 1726:v 1709:. 1705:: 1699:3 1682:. 1678:: 1672:3 1656:. 1590:. 1584:: 1557:) 1543:. 1539:: 1514:. 1510:: 1504:1 1487:. 1465:: 1429:. 1425:: 1397:. 1361:. 1349:: 1325:. 1313:: 1297:n 1284:. 1280:: 1261:. 1257:: 1229:. 1215:: 1196:. 1142:. 1125:o 1112:2 1098:2 1094:5 1092:H 1090:6 1086:2 1082:5 1080:H 1078:6 1057:2 1055:) 1053:3 1049:2 1040:3 1038:) 1036:3 1032:3 1030:) 1028:3 1024:4 1022:H 1020:6 1016:6 1014:) 1012:3 1008:2 1004:4 1002:H 1000:6 862:3 858:2 856:) 854:3 850:2 846:3 842:2 840:) 838:3 831:O 829:2 825:2 821:2 819:) 817:3 813:3 804:2 800:5 796:3 738:n 734:n 693:Y 493:D 396:2 392:3 293:) 289:( 138:) 20:)

Index

Palladium acetate




IUPAC name
CAS Number
3375-31-3
JSmol
Interactive image
Interactive image
ChemSpider
146827
ECHA InfoCard
100.020.151
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EC Number
PubChem
167845
RTECS number
UNII
0LTG3460Y5
CompTox Dashboard
DTXSID10890575
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Density

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