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Ammonia borane

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35: 1044: 1037: 871: 250: 157: 1002: 844: 1030: 1016: 1009: 454: 449: 44: 669: 836:. The B−N distance is 1.58(2) Å. The B−H and N−H distances are 1.15 and 0.96 Å, respectively. Its similarity to ethane is tenuous since ammonia borane is a solid and ethane is a gas: their melting points differing by 284 °C. This difference is consistent with the highly polar nature of ammonia borane. The H atoms attached to boron are 1272:
is prepared by the reaction of sodium borohydride with t-butylammonium chloride. Generally adduct are more robust with more basic amines. Variations are also possible for the boron component, although primary and secondary boranes are less common.
462: 429: 564: 1425: 682: 863:. The original crystallographic analysis of this compound reversed the assignments of B and N. The updated structure was arrived at with improved data using the technique of 1652:
Klooster, W. T.; Koetzle, T. F.; Siegbahn, P. E. M.; Richardson, T. B.; Crabtree, R. H. (1999). "Study of the N−H···H−B Dihydrogen Bond Including the Crystal Structure of BH
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Frueh, S.; Kellett, R.; Mallery, C.; Molter; T.; Willis, W. S.; King'ondu, C.; Suib, S. L. (2011). "Pyrolytic Decomposition of Ammonia Borane to Boron Nitride".
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Ramachandran, P. Veeraraghavan; Mistry, Hitesh; Kulkarni, Ameya S.; Gagare, Pravin D. (2014). "Ammonia-mediated, large-scale synthesis of ammonia borane".
870: 2035: 1163:(BN) at temperatures above 1000 °C. It is more hydrogen-dense than liquid hydrogen and also able to exist at normal temperatures and pressures. 560: 34: 1662: 2503: 516: 1380:
Umemoto, Hironobu; Miyata, Atsushi (2015). "Decomposition processes of diborane and borazane (ammonia-borane complex) on hot wire surfaces".
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Hu, M.G.; Van Paasschen, J.M.; Geanangel, R.A. (January 1977). "New synthetic approaches to ammonia-borane and its deuterated derivatives".
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centers. The closest H−H distance is 1.990 Å, which can be compared with the H−H bonding distance of 0.74 Å. This interaction is called a
1960: 1698: 1768: 264: 1133:, e.g. for when the gas is used to fuel motor vehicles. It can be made to release hydrogen on heating, being polymerized first to 1124: 1804: 1724: 1579:
Staubitz, Anne; Robertson, Alasdair P. M.; Manners, Ian (2010). "Ammonia-Borane and Related Compounds as Dihydrogen Sources".
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Sugie, Masaaki; Takeo, Harutoshi; Matsumura, Chi (1987). "Microwave spectrum and molecular structure of aminoborane, BH
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Bowden, Mark E.; Gainsford, Graeme J.; Robinson, Ward T. (2007). "Room-Temperature Structure of Ammonia Borane".
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Thorne, L. R.; Suenram, R. D.; Lovas, F. J. (1983). "Microwave spectrum, torsional barrier, and structure of BH
1043: 1036: 524: 592: 448: 1102: 536: 152: 1839: 1317: 1282: 1171: 1001: 114: 2417: 2138: 2126: 1110: 476: 441: 389: 56: 1978:"Ammonia borane-enabled hydrogen transfer processes: Insights into catalytic strategies and mechanisms" 1029: 1015: 1008: 2453: 2425: 1989: 1944: 1812: 1776: 1732: 1389: 1023: 245: 864: 540: 80: 588: 552: 520: 2161: 2100: 1935:
Andrews, Glenn C.; Neelamkavil, Santhosh F. (2008). "Borane–Ammonia". In Paquette, Leo A. (ed.).
945: 893: 817: 628: 584: 528: 401: 544: 2110: 2092: 1956: 1917: 1878: 1694: 1631: 1596: 1558: 1167: 713: 377: 2498: 2084: 1997: 1948: 1909: 1870: 1820: 1784: 1740: 1671: 1623: 1588: 1550: 1523: 1496: 1405: 1397: 1300: 1175: 596: 309: 134: 1449: 576: 216: 90: 2469: 2437: 2279: 2181: 2118: 2068: 2044: 860: 556: 1993: 1816: 1780: 1736: 1393: 782:(diammoniodihydroboronium tetrahydroborate). Ammonia borane is the main product when an 249: 156: 2445: 2383: 2359: 2350: 2327: 2303: 2291: 2267: 2058: 1802:
Kawashima, Yoshiyuki (1987). "Detection of HBNH by infrared diode laser spectroscopy".
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Boese, R.; Niederprüm, N.; Bläser, D. (1992). Maksic, Z. B.; Eckert-Masic, M. (eds.).
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Stephens, F. H.; Pons, V.; Baker, R. T. (2007). "Ammonia–Borane: The Hydrogen Source
1788: 1527: 1160: 840:(negatively charged) and those attached to nitrogen are acidic (positively charged). 833: 361: 145: 608: 572: 17: 2189: 940: 532: 196: 1952: 2255: 2219: 1976:
Zhao, Wenfeng; Li, Hu; Zhang, Heng; Yang, Song; Riisager, Anders (August 2023).
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as an air-stable derivative of diborane. It can be used as a reducing agent in
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that allowed the hydrogen atoms to be located with greater precision.
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Many analogues have been prepared from primary, secondary, and even
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Except where otherwise noted, data are given for materials in their
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Shore, S. G.; Boddeker, K. W. (1964). "Large Scale Synthesis of H
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The structure of the solid indicates a close association of the N
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Comparison of bond lengths in simple boron-nitrogen hydrides
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Ammonia borane has been suggested as a storage medium for
727:. The colourless or white solid is the simplest molecular 743:
fuel, but is otherwise primarily of academic interest.
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compound. It has attracted attention as a source of
2416: 2396: 2343: 2202: 2154: 2077: 2051: 828:The molecule adopts a structure similar to that of 1264:The first amine adduct of borane was derived from 195: 874:Part of the crystal structure of ammonia borane 89: 1937:Encyclopedia of Reagents for Organic Synthesis 2029: 8: 786:of borane is employed in place of diborane: 1647: 1645: 2036: 2022: 2014: 1516:Journal of Inorganic and Nuclear Chemistry 248: 155: 133: 26: 2001: 1691:Molecules in Natural Science and Medicine 1409: 215: 1663:Journal of the American Chemical Society 1344: 1331: 1327: 1323: 1310: 1306: 1256: 1252: 1248: 1244: 1234: 1230: 1226: 1212: 1208: 1204: 1200: 1153: 1144: 1140: 1136: 929: 921: 913: 877: 808: 804: 800: 792: 776: 770: 766: 762: 723: 719: 321: 317: 1574: 1572: 1358: 294: 269: 244: 1693:. Chichester, England: Ellis Horwood. 1174:reactions, often in the presence of a 847:Resonance structures of ammonia-borane 366:104 °C (219 °F; 377 K) 146: 276:Key: PJYXJGDRFASJSB-UHFFFAOYSA-N 7: 1051:Hybridisation of boron and nitrogen 186: 759:mainly gives the diammoniate salt 25: 1840:"Features: Hydrogen gets onboard" 1838:Gutowski, M.; Autrey, T. (2006). 1166:Ammonia borane finds some use in 1159:, which ultimately decomposes to 1125:Dehydrogenation of amine-boranes 1042: 1035: 1028: 1014: 1007: 1000: 816:It can also be synthesized from 667: 452: 447: 42: 33: 1616:Australian Journal of Chemistry 1367:"Method for producing borazane" 1099:Structure determination method 663:(at 25 °C , 100 kPa). 1982:Green Energy & Environment 1270:Borane tert-butylamine complex 1085:Proportion of B-N single bond 1: 1953:10.1002/047084289X.rb238.pub2 1789:10.1016/0022-2852(87)90279-7 1528:10.1016/0022-1902(77)80383-7 977:Analogous hydrocarbon class 704:(also systematically named 2525: 1122: 2344:Boron oxides and sulfides 2003:10.1016/j.gee.2022.03.011 1660:by Neutron Diffraction". 1402:10.1016/j.tsf.2015.04.084 657: 614: 428: 423: 370: 302: 285: 273:InChI=1S/BH6N/c1-2/h1-2H3 260: 73: 65: 55: 50: 41: 32: 2504:Boron–nitrogen compounds 824:Properties and structure 511:Precautionary statements 1241:Borane isopropylamine ( 1182:Analogous amine-boranes 1107:microwave spectroscopy 407:Tetrahedral at B and N 1426:"Results for Borazane" 1339:Borane–tetrahydrofuran 1318:Borane dimethylsulfide 1283:Tert-butylamine borane 1195:Borane tert-butylamine 1172:transfer hydrogenation 1103:microwave spectroscopy 957:Analogous hydrocarbon 875: 848: 395:Tetragonal at B and N 2418:Organoboron compounds 1945:John Wiley & Sons 1111:infrared spectroscopy 873: 846: 706:ammoniotrihydroborate 390:Coordination geometry 60:Ammoniotrihydroborate 1024:Ball-and-stick model 18:Amine borane complex 2494:Inorganic compounds 2052:Boron pnictogenides 1994:2023GrEE....8..948Z 1902:Dalton Transactions 1863:Inorganic Chemistry 1817:1987JChPh..87.6331K 1781:1987JMoSp.123..286S 1737:1983JChPh..78..167T 1549:(44): 16580–16583. 1501:10.1021/ic50016a038 1489:Inorganic Chemistry 1394:2015TSF...595..231U 880: 865:neutron diffraction 832:, with which it is 346:Colorless crystals 338: g·mol 29: 1769:J. Mol. Spectrosc. 1555:10.1039/C4DT02467B 878: 876: 849: 818:sodium borohydride 690:Infobox references 629:Sodium borohydride 615:Related compounds 27: 2481: 2480: 1908:(25): 2613–2626. 1875:10.1021/ic101020k 1811:(11): 6331–6333. 1676:10.1021/ja9825332 1670:(27): 6337–6343. 1593:10.1021/cr100088b 1522:(12): 2147–2150. 1168:organic synthesis 1116: 1115: 716:with the formula 714:chemical compound 698:Chemical compound 696: 695: 621:Related compounds 477:Hazard statements 383:I4mm, tetragonal 378:Crystal structure 229:CompTox Dashboard 115:Interactive image 16:(Redirected from 2516: 2509:Inorganic amines 2038: 2031: 2024: 2015: 2008: 2007: 2005: 1973: 1967: 1966: 1932: 1926: 1925: 1914:10.1039/b703053c 1893: 1887: 1886: 1858: 1852: 1851: 1835: 1829: 1828: 1825:10.1063/1.453462 1799: 1793: 1792: 1755: 1749: 1748: 1745:10.1063/1.444528 1711: 1705: 1704: 1686: 1680: 1679: 1649: 1640: 1639: 1611: 1605: 1604: 1587:(7): 4079–4124. 1581:Chemical Reviews 1576: 1567: 1566: 1538: 1532: 1531: 1511: 1505: 1504: 1460: 1454: 1453: 1450:"Ammonia borane" 1446: 1440: 1439: 1437: 1436: 1430:sigmaaldrich.com 1422: 1416: 1415: 1413: 1382:Thin Solid Films 1377: 1371: 1370: 1363: 1347: 1334: 1313: 1301:Phosphine-borane 1259: 1237: 1215: 1176:transition metal 1158: 1149: 1065:B-N bond length 1046: 1039: 1032: 1018: 1011: 1004: 932: 924: 916: 881: 812: 781: 726: 680: 674: 671: 670: 610: 606: 602: 598: 594: 590: 586: 582: 578: 574: 570: 566: 562: 558: 554: 550: 546: 542: 538: 534: 530: 526: 522: 518: 504: 500: 496: 492: 488: 484: 456: 451: 337: 324: 310:Chemical formula 253: 252: 237: 235: 219: 199: 188: 167: 159: 148: 137: 117: 93: 46: 37: 30: 21: 2524: 2523: 2519: 2518: 2517: 2515: 2514: 2513: 2484: 2483: 2482: 2477: 2473: 2465: 2461: 2457: 2449: 2441: 2433: 2429: 2412: 2407: 2392: 2387: 2379: 2375: 2367: 2363: 2354: 2339: 2335: 2331: 2323: 2319: 2311: 2307: 2299: 2295: 2287: 2283: 2275: 2271: 2263: 2259: 2251: 2247: 2239: 2235: 2227: 2223: 2215: 2198: 2193: 2185: 2177: 2169: 2165: 2150: 2146: 2142: 2134: 2130: 2122: 2114: 2096: 2088: 2073: 2047: 2045:Boron compounds 2042: 2012: 2011: 1975: 1974: 1970: 1963: 1934: 1933: 1929: 1895: 1894: 1890: 1860: 1859: 1855: 1844:Chemistry World 1837: 1836: 1832: 1801: 1800: 1796: 1765: 1761: 1757: 1756: 1752: 1721: 1717: 1713: 1712: 1708: 1701: 1688: 1687: 1683: 1659: 1655: 1651: 1650: 1643: 1628:10.1071/ch06442 1613: 1612: 1608: 1578: 1577: 1570: 1540: 1539: 1535: 1513: 1512: 1508: 1486: 1482: 1478: 1474: 1470: 1466: 1462: 1461: 1457: 1448: 1447: 1443: 1434: 1432: 1424: 1423: 1419: 1379: 1378: 1374: 1365: 1364: 1360: 1355: 1346: 1342: 1333: 1329: 1325: 1321: 1312: 1308: 1304: 1296: 1292: 1279: 1258: 1254: 1250: 1246: 1242: 1236: 1232: 1228: 1224: 1214: 1210: 1206: 1202: 1198: 1188:tertiary amines 1184: 1157: 1151: 1148: 1142: 1138: 1134: 1127: 1121: 931: 927: 923: 919: 915: 911: 861:dihydrogen bond 826: 810: 806: 802: 794: 790: 778: 772: 768: 764: 760: 749: 725: 721: 717: 708:), also called 699: 692: 687: 686: 685:  ?) 676: 672: 668: 664: 653: 622: 513: 479: 465: 444: 416: 404: 402:Molecular shape 392: 380: 335: 323: 319: 315: 312: 298: 293: 292: 281: 278: 277: 274: 268: 267: 256: 238: 231: 222: 202: 189: 177: 140: 120: 107: 96: 83: 69: 61: 28:Ammonia borane 23: 22: 15: 12: 11: 5: 2522: 2520: 2512: 2511: 2506: 2501: 2496: 2486: 2485: 2479: 2478: 2476: 2475: 2471: 2467: 2463: 2459: 2455: 2451: 2447: 2443: 2439: 2435: 2431: 2427: 2422: 2420: 2414: 2413: 2411: 2410: 2405: 2400: 2398: 2394: 2393: 2391: 2390: 2385: 2381: 2377: 2373: 2369: 2365: 2361: 2357: 2352: 2347: 2345: 2341: 2340: 2338: 2337: 2333: 2329: 2325: 2321: 2317: 2313: 2309: 2305: 2301: 2297: 2293: 2289: 2285: 2281: 2277: 2273: 2269: 2265: 2261: 2257: 2253: 2249: 2245: 2241: 2237: 2233: 2229: 2225: 2221: 2217: 2213: 2208: 2206: 2200: 2199: 2197: 2196: 2191: 2187: 2183: 2179: 2175: 2171: 2167: 2163: 2158: 2156: 2152: 2151: 2149: 2148: 2144: 2140: 2136: 2132: 2128: 2124: 2120: 2116: 2112: 2108: 2103: 2098: 2094: 2090: 2086: 2081: 2079: 2075: 2074: 2072: 2071: 2066: 2061: 2055: 2053: 2049: 2048: 2043: 2041: 2040: 2033: 2026: 2018: 2010: 2009: 1988:(4): 948–971. 1968: 1962:978-0471936237 1961: 1927: 1898:par excellence 1888: 1869:(3): 783–792. 1853: 1830: 1805:J. Chem. Phys. 1794: 1775:(2): 286–292. 1763: 1759: 1750: 1731:(1): 167–171. 1725:J. Chem. Phys. 1719: 1715: 1706: 1700:978-0135615980 1699: 1681: 1657: 1653: 1641: 1606: 1568: 1533: 1506: 1495:(6): 914–915. 1484: 1480: 1476: 1472: 1468: 1464: 1455: 1441: 1417: 1372: 1357: 1356: 1354: 1351: 1350: 1349: 1336: 1315: 1298: 1294: 1290: 1278: 1275: 1266:trimethylamine 1262: 1261: 1239: 1221:trimethylamine 1217: 1183: 1180: 1123:Main article: 1120: 1117: 1114: 1113: 1108: 1105: 1100: 1096: 1095: 1092: 1089: 1086: 1082: 1081: 1076: 1071: 1066: 1062: 1061: 1058: 1055: 1052: 1048: 1047: 1040: 1033: 1026: 1020: 1019: 1012: 1005: 998: 994: 993: 988: 983: 978: 974: 973: 968: 963: 958: 954: 953: 948: 943: 938: 934: 933: 925: 917: 909: 905: 904: 897: 890: 888:Ammonia borane 885: 825: 822: 814: 813: 748: 745: 702:Ammonia borane 697: 694: 693: 688: 666: 665: 661:standard state 658: 655: 654: 652: 651: 646: 641: 636: 631: 625: 623: 620: 617: 616: 612: 611: 565:P305+P351+P338 514: 509: 506: 505: 480: 475: 472: 471: 466: 461: 458: 457: 445: 440: 437: 436: 426: 425: 421: 420: 417: 412: 409: 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Retrieved 1429: 1420: 1385: 1381: 1375: 1361: 1286: 1263: 1185: 1165: 1154: 1145: 1128: 1078: 1073: 1068: 941:amine-borane 899: 892: 887: 856: 852: 850: 827: 815: 751:Reaction of 750: 709: 705: 701: 700: 468: 430: 74:Identifiers 66:Other names 1411:10297/10128 1388:: 231–234. 951:iminoborane 946:aminoborane 901:Iminoborane 894:Aminoborane 463:Signal word 343:Appearance 303:Properties 153:100.170.890 2488:Categories 1622:(3): 149. 1435:2024-09-06 1353:References 1178:catalyst. 1150:, then to 997:Structure 442:Pictograms 371:Structure 356:0.78 g/cm 331:Molar mass 217:XR7O5A5MH6 126:ChemSpider 102:3D model ( 91:13774-81-7 81:CAS Number 57:IUPAC name 1636:0004-9425 971:acetylene 884:Molecule 855:and the B 747:Synthesis 712:, is the 601:P403+P233 597:P370+P378 593:P362+P364 589:P337+P317 585:P332+P317 561:P304+P340 557:P302+P352 553:P301+P317 537:P264+P265 433:labelling 174:642-983-4 166:EC Number 2397:Carbides 1941:New York 1922:17576485 1883:21182274 1601:20672860 1563:25274135 1277:See also 1131:hydrogen 966:ethylene 908:Formula 838:hydridic 753:diborane 741:hydrogen 733:nitrogen 710:borazane 644:Diborane 634:Borazine 424:Hazards 68:Borazane 2499:Boranes 2204:Boranes 1990:Bibcode 1813:Bibcode 1777:Bibcode 1733:Bibcode 1390:Bibcode 1219:Borane 1079:1.238 Å 1074:1.391 Å 1069:1.658 Å 775:[BH 757:ammonia 737:hydride 683:what is 681: ( 352:Density 325: 184:PubChem 1959:  1920:  1881:  1697:  1634:  1599:  1561:  1343:THF→BH 1152:(NHBH) 991:alkyne 986:alkene 981:alkane 961:ethane 937:Class 830:ethane 799:) + NH 784:adduct 761:[H 678:verify 675:  649:Ethane 639:Borane 469:Danger 419:5.2 D 290:SMILES 197:419330 135:371215 51:Names 2174:B(OH) 2155:Acids 1479:and H 1251:CH−NH 1088:100% 811:+ THF 755:with 729:boron 336:30.87 265:InChI 104:JSmol 2470:COBH 2162:B(NO 1957:ISBN 1918:PMID 1906:2007 1900:?". 1879:PMID 1850:(3). 1695:ISBN 1632:ISSN 1597:PMID 1559:PMID 1467:B(NH 1330:S→BH 1309:P→BH 1289:BuNH 1233:N→BH 1207:C−NH 1119:Uses 1094:75% 1091:84% 803:→ BH 765:B(NH 609:P501 605:P405 581:P330 577:P321 573:P319 569:P317 549:P280 545:P271 541:P270 533:P264 529:P261 525:P241 521:P240 517:P210 503:H335 499:H332 495:H319 491:H315 487:H302 483:H228 208:UNII 2458:(BO 2446:BEt 2438:BMe 2430:Me) 2426:(BH 2182:BPO 2106:BFO 2093:BCl 2085:BBr 2059:BAs 1998:doi 1949:doi 1910:doi 1871:doi 1821:doi 1785:doi 1773:123 1766:". 1741:doi 1722:". 1672:doi 1668:121 1624:doi 1589:doi 1585:110 1551:doi 1524:doi 1497:doi 1487:". 1483:NBH 1406:hdl 1398:doi 1386:595 1322:(CH 1293:→BH 1255:→BH 1243:(CH 1225:(CH 1211:→BH 1199:(CH 1135:(NH 1060:sp 1057:sp 1054:sp 928:BNH 920:BNH 912:BNH 797:THF 722:NBH 431:GHS 320:NBH 234:EPA 187:CID 2490:: 2454:Ac 2334:22 2330:18 2322:14 2318:10 2310:12 2298:10 2286:11 2262:10 2248:NH 2244:BH 2212:BH 2190:BH 2143:Cl 2119:BI 2111:BF 2101:BF 2069:BP 2064:BN 1996:. 1984:. 1980:. 1955:. 1947:. 1943:: 1939:. 1916:. 1904:. 1877:. 1867:50 1865:. 1846:. 1842:. 1819:. 1809:87 1783:. 1762:NH 1739:. 1729:78 1718:NH 1666:. 1656:NH 1644:^ 1630:. 1620:60 1618:. 1595:. 1583:. 1571:^ 1557:. 1547:43 1545:. 1520:39 1518:. 1491:. 1475:BH 1428:. 1404:. 1396:. 1268:. 1190:: 1139:BH 820:. 807:NH 791:BH 607:, 603:, 599:, 595:, 591:, 587:, 583:, 579:, 575:, 571:, 567:, 563:, 559:, 555:, 551:, 547:, 543:, 539:, 535:, 531:, 527:, 523:, 519:, 501:, 497:, 493:, 489:, 485:, 435:: 2472:3 2464:2 2462:) 2460:3 2456:4 2448:3 2440:3 2432:2 2428:2 2408:C 2406:4 2404:B 2388:O 2386:6 2384:B 2378:3 2376:S 2374:2 2372:B 2366:3 2364:O 2362:2 2360:B 2355:O 2353:2 2351:B 2332:H 2328:B 2320:H 2316:B 2308:H 2306:6 2304:B 2296:H 2294:6 2292:B 2284:H 2282:5 2280:B 2274:9 2272:H 2270:5 2268:B 2260:H 2258:4 2256:B 2250:3 2246:3 2238:6 2236:H 2234:2 2232:B 2226:4 2224:H 2222:2 2220:B 2214:3 2194:O 2192:3 2184:4 2176:3 2168:3 2166:) 2164:3 2145:4 2141:2 2139:B 2133:4 2131:F 2129:2 2127:B 2121:3 2113:3 2095:3 2087:3 2037:e 2030:t 2023:v 2006:. 2000:: 1992:: 1986:8 1965:. 1951:: 1924:. 1912:: 1885:. 1873:: 1848:3 1827:. 1823:: 1815:: 1791:. 1787:: 1779:: 1764:2 1760:2 1747:. 1743:: 1735:: 1720:3 1716:3 1703:. 1678:. 1674:: 1658:3 1654:3 1638:. 1626:: 1603:. 1591:: 1565:. 1553:: 1530:. 1526:: 1503:. 1499:: 1493:3 1485:3 1481:3 1477:4 1473:2 1471:) 1469:3 1465:2 1452:. 1438:. 1414:. 1408:: 1400:: 1392:: 1369:. 1348:) 1345:3 1341:( 1335:) 1332:3 1328:2 1326:) 1324:3 1320:( 1314:) 1311:3 1307:3 1305:R 1303:( 1297:) 1295:3 1291:2 1287:t 1285:( 1260:) 1257:3 1253:2 1249:2 1247:) 1245:3 1238:) 1235:3 1231:3 1229:) 1227:3 1223:( 1216:) 1213:3 1209:2 1205:3 1203:) 1201:3 1197:( 1155:n 1146:n 1143:) 1141:2 1137:2 930:2 922:4 914:6 857:H 853:H 809:3 805:3 801:3 795:( 793:3 779:] 777:4 773:] 771:2 769:) 767:3 763:2 735:- 731:- 724:3 720:3 718:H 673:N 322:3 318:3 316:H 236:) 232:( 106:) 20:)

Index

Amine borane complex
Ball and stick model of ammonia borane

IUPAC name
CAS Number
13774-81-7
JSmol
Interactive image
ChemSpider
371215
ECHA InfoCard
100.170.890
Edit this at Wikidata
EC Number
PubChem
419330
UNII
XR7O5A5MH6
CompTox Dashboard
DTXSID40422702
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InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
Crystal structure
Coordination geometry
Molecular shape

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