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Brar, Sukhwinder Singh; Mahajan, Aman; Bedi, R. K. (10 January 2014). "Structural, optical and electrical characterization of hot wall grown 9,10-dibromoanthracene films for light emitting applications".
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substrate on which the 9,10-dibromoanthracene reactant was placed. Further voltage pulses cause the diradical to convert to a diyne (or back again) via a
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atoms substituted on its central ring. It is notable in that it was the first single molecule to have a chemical reaction observed by an
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can be fragmented in two successive steps by voltage pulses from tip of a scanning tunneling microscope. The resulting carbon
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and John S. Heaton were the first to synthesize this in 1923 in
England.
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InChI=1S/C14H8Br2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
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Except where otherwise noted, data are given for materials in their
668:"Chemists Nudge Molecule To React Then Watch Bonds Break And Form"
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520:is an organic chemical compound containing
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670:. Vol. 94, no. 5. p. 7.
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265:Key: BRUOAURMAFDGLP-UHFFFAOYSA-N
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286:C1=CC=C2C(=C1)C(=C3C=CC=CC3=C2Br)Br
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502:(at 25 °C , 100 kPa).
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1:
534:scanning tunneling microscopy
633:Electronic Materials Letters
559:, giving off a blue light.
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555:9,10-Dibromoanthracene is
645:10.1007/s13391-013-3153-8
617:American Chemical Society
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613:"9,10-Dibromoanthracene"
421:Precautionary statements
530:atomic force microscope
17:9,10-Dibromoanthracene
575:are stabilized by the
518:9,10-Dibromoanthracene
41:9,10-Dibromoanthracene
666:Borman, Stu (2016).
569:carbon–bromine bonds
37:Preferred IUPAC name
581:Bergman cyclization
337: g·mol
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557:electroluminescent
506:Infobox references
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514:Chemical compound
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395:Hazard statements
223:CompTox Dashboard
89:Interactive image
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302:Chemical formula
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639:(1): 199–204.
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500:standard state
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455:P305+P351+P338
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141:ECHA InfoCard
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109:ChEMBL3183379
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48:Identifiers
693:Anthracenes
688:Bromoarenes
381:Signal word
295:Properties
147:100.007.586
682:Categories
596:References
583:reaction.
551:Properties
540:Production
522:anthracene
360:Pictograms
330:Molar mass
211:61CP7C5Y82
120:ChemSpider
76:3D model (
55:CAS Number
653:135788635
563:Reactions
524:with two
483:P403+P233
471:P337+P313
467:P332+P313
451:P304+P340
447:P302+P352
351:labelling
168:208-342-4
160:EC Number
573:radicals
342:Hazards
65:523-27-3
526:bromine
387:Warning
335:336.026
178:PubChem
651:
279:SMILES
100:ChEMBL
31:Names
649:S2CID
254:InChI
191:68226
129:61529
78:JSmol
567:The
532:and
491:P501
487:P405
479:P391
475:P362
463:P321
459:P312
443:P280
439:P273
435:P271
431:P264
427:P261
413:H410
409:H335
405:H319
401:H315
202:UNII
641:doi
349:GHS
228:EPA
181:CID
684::
647:.
637:10
635:.
615:.
604:^
536:.
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411:,
407:,
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353::
320:Br
311:14
655:.
643::
619:.
323:2
317:8
314:H
308:C
230:)
226:(
80:)
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