Knowledge (XXG)

Organoastatine chemistry

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procedures are used today, first synthesising stable astatoaryl prosthetic groups before incorporating them into the protein. Not only is the C–At bond the weakest of all carbon–halogen bonds (following periodic trends), but also the bond easily breaks as the astatine is oxidised back to free astatine.
79:). Alkyl and aryl astatides are relatively stable and have been analysed at high temperatures (120 Â°C) with radio gas chromatography. Demercuration reactions have produced with good yields trace quantities of At-containing aromatic amino acids, steroids, and imidazoles, among other compounds. 87:
group), halodeprotonation, or halodemetallation. Initial attempts to radiolabel proteins with At exemplify its intermediate behaviour, as astatination (analogous to radioiodination) produces unstable results and it is instead AtO (or a hydrolysed species) that probably bonds to proteins. Two-step
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Astatine is extremely radioactive, with the longest-lived isotope (At) having a half-life of only 8.1 hours. Consequently, organoastatine chemistry can only be studied by tracer techniques on extremely small quantities. The problems caused by radiation damage as well as difficulties in
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Astatine has both halogen-like and metallic properties, so that analogies with iodine sometimes hold, but sometimes do not. Astatine can be incorporated into organic molecules via halogen exchange, halodediazotation (replacing a
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separation and identification are worse for organic astatine derivatives than for inorganic compounds. Most studies of organoastatine chemistry focus on At (half-life 7.21 hours), which is the subject of ongoing studies in
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Guérard, François; Maingueneau, Clémence; Liu, Lu; Eychenne, Romain; Gestin, Jean-François; Montavon, Gilles; Galland, Nicolas (2021).
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Coenen, H. H.; Moerlein, S. M.; Stöcklin, G. (1983). "No-Carrier-Added Radiohalogenation Methods with Heavy Halogens".
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Astatine-labelled iodine reagents have been used to synthesise RAt, RAtCl
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(1983). 1: 189:Accounts of Chemical Research 201:10.1021/acs.accounts.1c00327 1063: 969: 156:10.1524/ract.1983.34.12.47 839: 758: 310: 306: 296: 115:Chemistry of the Elements 113:; Earnshaw, Alan (1997). 1042:Organometallic chemistry 24:organoastatine compounds 20:Organoastatine chemistry 53:at destroying abnormal 986:-related article is a 945:Many uses in chemistry 940:Core organic chemistry 119:Butterworth-Heinemann 111:Greenwood, Norman N. 121:. pp. 885–887. 49:: it is better than 28:chemical compounds 999: 998: 964: 963: 920: 919: 195:(16): 3264–3275. 144:Radiochimica Acta 128:978-0-08-037941-8 1054: 1020: 1013: 1006: 978: 971: 956: 951: 946: 941: 846: 845: 765: 764: 697: 696: 602: 601: 299: 281: 274: 267: 258: 253: 251: 249: 240: 221: 220: 186: 177: 168: 167: 139: 133: 132: 117:(2nd ed.). 107: 47:nuclear medicine 1062: 1061: 1057: 1056: 1055: 1053: 1052: 1051: 1047:Chemistry stubs 1027: 1026: 1025: 1024: 967: 965: 960: 959: 954: 949: 944: 939: 921: 843: 762: 694: 599: 292: 285: 247: 245: 238: 233: 230: 228:Further reading 225: 224: 184: 179: 178: 171: 141: 140: 136: 129: 109: 108: 99: 94: 72:(R = phenyl or 71: 67: 63: 17: 12: 11: 5: 1060: 1058: 1050: 1049: 1044: 1039: 1029: 1028: 1023: 1022: 1015: 1008: 1000: 997: 996: 979: 962: 961: 958: 957: 952: 947: 942: 937: 934:Chemical bonds 930: 929: 927: 923: 922: 918: 917: 912: 907: 902: 897: 892: 887: 882: 877: 872: 867: 862: 857: 852: 847: 840: 837: 836: 831: 826: 821: 816: 811: 806: 801: 796: 791: 786: 781: 776: 771: 766: 759: 756: 755: 751: 750: 747: 744: 741: 738: 735: 732: 729: 726: 723: 720: 717: 714: 709: 706: 703: 698: 691: 686: 682: 681: 678: 673: 668: 663: 658: 653: 648: 643: 638: 633: 628: 623: 618: 613: 608: 603: 596: 591: 585: 584: 579: 574: 569: 564: 559: 554: 549: 544: 539: 534: 529: 524: 519: 514: 509: 504: 502: 497: 491: 490: 485: 480: 475: 470: 465: 460: 455: 450: 445: 440: 435: 430: 425: 420: 415: 410: 408: 403: 397: 396: 391: 386: 381: 376: 371: 366: 361: 355: 354: 351: 346: 341: 336: 331: 326: 321: 315: 314: 311: 309: 307: 305: 297: 294: 293: 286: 284: 283: 276: 269: 261: 255: 254: 229: 226: 223: 222: 169: 150:(1–2): 47–68. 134: 127: 96: 95: 93: 90: 69: 68:AtCl, and RAtO 65: 61: 15: 13: 10: 9: 6: 4: 3: 2: 1059: 1048: 1045: 1043: 1040: 1038: 1035: 1034: 1032: 1021: 1016: 1014: 1009: 1007: 1002: 1001: 995: 993: 989: 985: 980: 977: 973: 968: 953: 948: 943: 938: 935: 932: 931: 928: 924: 916: 913: 911: 908: 906: 903: 901: 898: 896: 893: 891: 888: 886: 883: 881: 878: 876: 873: 871: 868: 866: 863: 861: 858: 856: 853: 851: 848: 841: 838: 835: 832: 830: 827: 825: 822: 820: 817: 815: 812: 810: 807: 805: 802: 800: 797: 795: 792: 790: 787: 785: 782: 780: 777: 775: 772: 770: 767: 760: 757: 753: 752: 748: 745: 742: 739: 736: 733: 730: 727: 724: 721: 718: 715: 713: 710: 707: 704: 702: 699: 692: 690: 687: 684: 683: 679: 677: 674: 672: 669: 667: 664: 662: 659: 657: 654: 652: 649: 647: 644: 642: 639: 637: 634: 632: 629: 627: 624: 622: 619: 617: 614: 612: 609: 607: 604: 597: 595: 592: 590: 587: 586: 583: 580: 578: 575: 573: 570: 568: 565: 563: 560: 558: 555: 553: 550: 548: 545: 543: 540: 538: 535: 533: 530: 528: 525: 523: 520: 518: 515: 513: 510: 508: 505: 503: 501: 498: 496: 493: 492: 489: 486: 484: 481: 479: 476: 474: 471: 469: 466: 464: 461: 459: 456: 454: 451: 449: 446: 444: 441: 439: 436: 434: 431: 429: 426: 424: 421: 419: 416: 414: 411: 409: 407: 404: 402: 399: 398: 395: 392: 390: 387: 385: 382: 380: 377: 375: 372: 370: 367: 365: 362: 360: 357: 356: 352: 350: 347: 345: 342: 340: 337: 335: 332: 330: 327: 325: 322: 320: 317: 316: 312: 304: 301: 300: 295: 290: 287:Compounds of 282: 277: 275: 270: 268: 263: 262: 259: 244: 243:inis.iaea.org 237: 232: 231: 227: 218: 214: 210: 206: 202: 198: 194: 190: 183: 176: 174: 170: 165: 161: 157: 153: 149: 145: 138: 135: 130: 124: 120: 116: 112: 106: 104: 102: 98: 91: 89: 86: 80: 78: 76: 58: 56: 52: 48: 42: 40: 39:chemical bond 37: 33: 30:containing a 29: 25: 21: 992:expanding it 981: 966: 955:Bond unknown 675: 246:. Retrieved 242: 192: 188: 147: 143: 137: 114: 81: 74: 59: 43: 23: 19: 18: 248:19 December 1031:Categories 92:References 984:chemistry 936:to carbon 217:236926712 85:diazonium 1037:Astatine 209:34350753 164:99845370 57:tissue. 36:astatine 754:  55:thyroid 926:Legend 289:carbon 215:  207:  162:  125:  77:-tolyl 32:carbon 982:This 239:(PDF) 213:S2CID 185:(PDF) 160:S2CID 988:stub 250:2022 205:PMID 123:ISBN 900:CEs 895:CCf 890:CBk 885:CCm 880:CAm 875:CPu 870:CNp 860:CPa 855:CTh 834:CYb 829:CTm 824:CEr 819:CHo 814:CDy 809:CTb 804:CGd 799:CEu 794:CSm 789:CPm 784:CNd 779:CPr 774:CCe 769:CLa 749:Og 746:Ts 743:Lv 740:Mc 737:Fl 734:Nh 731:Cn 728:Rg 725:Ds 722:Mt 719:Hs 716:Bh 712:CSg 708:Db 705:Rf 689:CRa 685:Fr 680:Rn 676:CAt 671:CPo 666:CBi 661:CPb 656:CTl 651:CHg 646:CAu 641:CPt 636:CIr 631:COs 626:CRe 616:CTa 611:CHf 606:CLu 594:CBa 589:CCs 582:CXe 572:CTe 567:CSb 562:CSn 557:CIn 552:CCd 547:CAg 542:CPd 537:CRh 532:CRu 527:CTc 522:CMo 517:CNb 512:CZr 500:CSr 495:CRb 488:CKr 483:CBr 478:CSe 473:CAs 468:CGe 463:CGa 458:CZn 453:CCu 448:CNi 443:CCo 438:CFe 433:CMn 428:CCr 418:CTi 413:CSc 406:CCa 394:CAr 389:CCl 374:CSi 369:CAl 364:CMg 359:CNa 353:Ne 324:CBe 319:CLi 313:He 197:doi 152:doi 64:, R 34:to 1033:: 915:No 910:Md 905:Fm 865:CU 850:Ac 701:Lr 621:CW 577:CI 507:CY 423:CV 401:CK 384:CS 379:CP 349:CF 344:CO 339:CN 334:CC 329:CB 303:CH 241:. 211:. 203:. 193:54 191:. 187:. 172:^ 158:. 148:34 146:. 100:^ 41:. 26:, 1019:e 1012:t 1005:v 994:. 280:e 273:t 266:v 252:. 219:. 199:: 166:. 154:: 131:. 75:p 70:2 66:2 62:2 51:I

Index

chemical compounds
carbon
astatine
chemical bond
nuclear medicine
I
thyroid
p-tolyl
diazonium



Greenwood, Norman N.
Butterworth-Heinemann
ISBN
978-0-08-037941-8
doi
10.1524/ract.1983.34.12.47
S2CID
99845370


"Advances in the Chemistry of Astatine and Implications for the Development of Radiopharmaceuticals"
doi
10.1021/acs.accounts.1c00327
PMID
34350753
S2CID
236926712
"Organic Chemistry of Astatine"

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