On the dual reactivity of a nucleophilic dihydrido-diborane: reaction at the B−B bond and/or the B−H bond
The electron-rich, double-base stabilized dihydrido-diborane(4) [HB(hpp)]2 (hpp=1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidinate) combines two different, easily accessible reactive sites: the B−B and B−H bond. Herein, we report two basically similar reactions of [HB(hpp)]2 with catecholborane an...
Gespeichert in:
| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2018
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| In: |
Chemistry - a European journal
Year: 2017, Jahrgang: 24, Heft: 5, Pages: 1209-1216 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.201705028 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1002/chem.201705028 Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201705028 
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| Verfasserangaben: | Anna Widera, Elisabeth Kaifer, Hubert Wadepohl, and Hans-Jörg Himmel |
MARC
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| 245 | 1 | 0 | |a On the dual reactivity of a nucleophilic dihydrido-diborane |b reaction at the B−B bond and/or the B−H bond |c Anna Widera, Elisabeth Kaifer, Hubert Wadepohl, and Hans-Jörg Himmel |
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| 520 | |a The electron-rich, double-base stabilized dihydrido-diborane(4) [HB(hpp)]2 (hpp=1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidinate) combines two different, easily accessible reactive sites: the B−B and B−H bond. Herein, we report two basically similar reactions of [HB(hpp)]2 with catecholborane and B-chlorocatecholborane unsuspectedly resulting in two different reactivities. While reaction of the diborane with two equivalents of HB(cat) proceeded with formation of a cationic triborane with a (3c2e) bond, [HB(μ-hpp)2(μ-BH2)]+, reaction with ClB(cat) led to hydride-chloride substitution yielding [ClB(hpp)]2. The cationic triborane was also obtained by the addition of BH3 to the in situ generated [HB(hpp)2B]+. Proceeding from the new compound [ClB(hpp)]2, we investigated its reactivity towards chloride abstraction with AlCl3 and GaCl3. Irrespectively of the salt chosen, the reaction led to formation of a radical tricationic tetraborane [B(hpp)4].3+ with a (4c,5e) bond. Moreover, the dichloro-diborane proves as a versatile reagent for further substitution cleanly reacting with the strong nucleophile nBuLi to a new dibutyl-diborane [nBuB(hpp)]2. | ||
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| 650 | 4 | |a boron | |
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| 650 | 4 | |a hydrides | |
| 650 | 4 | |a nucleophiles | |
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