Strong metal-borane interactions in low-valent cyclopentadienyl rhodium complexes
The first examples of half-sandwich Rh( i ) complexes stabilized by borane coordination have been prepared and structurally characterized. As substantiated by NMR spectroscopy and single-crystal X-ray diffraction, the phosphine-borane ligand iPr 2 P-( o -C 6 H 4 )-BFxyl 2 1 [Fxyl = 3,5-(F 3 C) 2 C 6...
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Published in | Chemical communications (Cambridge, England) Vol. 55; no. 85; pp. 12837 - 1284 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
22.10.2019
|
Subjects | |
Online Access | Get full text |
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Summary: | The first examples of half-sandwich Rh(
i
) complexes stabilized by borane coordination have been prepared and structurally characterized. As substantiated by NMR spectroscopy and single-crystal X-ray diffraction, the phosphine-borane ligand iPr
2
P-(
o
-C
6
H
4
)-BFxyl
2
1 [Fxyl = 3,5-(F
3
C)
2
C
6
H
3
] engages in tight η
3
-BCC or η
1
-B coordination, depending on the metal environment.
Half-sandwich Rh(
i
) complexes stabilized by η
3
-BCC or η
1
-B borane coordination. |
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Bibliography: | Electronic supplementary information (ESI) available: Experimental procedures and characterization of complexes ( ) 1938719 1938717 1938718 For ESI and crystallographic data in CIF or other electronic format see DOI 2 3 4 10.1039/c9cc06639j and 2-5 (PDF). CCDC ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c9cc06639j |