1993
DOI: 10.1039/dt9930000723
|View full text |Cite
|
Sign up to set email alerts
|

Reactivity of the [ReNR]3+and [ReN]2+cores toward bis(diphenylphosphino)amine and its derivatives. Synthesis and crystal structures

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

2
25
0

Year Published

1994
1994
2015
2015

Publication Types

Select...
7
1
1

Relationship

1
8

Authors

Journals

citations
Cited by 64 publications
(27 citation statements)
references
References 12 publications
(1 reference statement)
2
25
0
Order By: Relevance
“…[11,12] The di-chalcogenoimido-diphosphinto bismuth compounds, Bi[(EPR 2 ) 2 N] 3 (E = S, Se; R = Ph, iPr), were found to be ideal www.zaac.wiley-vch.de ARTICLE for use as single-source precursors as they are air-stable and readily obtainable in good synthetic yields. [13] The diselenoimido-diphosphinato ligand can also stabilize a wide range of metal coordination spheres including alkali metals, [14][15] group 12, [16] group 13, [17,18] group 14, [19,20,16] group 15, [21] group 16, [22,23] transition metals (V and Cr, [24] Mn [25,26] and Re, [27] Ru, Rh, Ir, [15,28,29] Os, [30] Co, [31] group 10: Ni, [32] Pd, [32,[33][34][35] Pt, [14,30,34] and group 11: [35] , and rare earth metals. [36,37] This could be due to the flexible nature of the ligand moieties, which adopt to several metallacyclic rings depending upon the coordination to the central metal atom.…”
Section: Introductionmentioning
confidence: 99%
“…[11,12] The di-chalcogenoimido-diphosphinto bismuth compounds, Bi[(EPR 2 ) 2 N] 3 (E = S, Se; R = Ph, iPr), were found to be ideal www.zaac.wiley-vch.de ARTICLE for use as single-source precursors as they are air-stable and readily obtainable in good synthetic yields. [13] The diselenoimido-diphosphinato ligand can also stabilize a wide range of metal coordination spheres including alkali metals, [14][15] group 12, [16] group 13, [17,18] group 14, [19,20,16] group 15, [21] group 16, [22,23] transition metals (V and Cr, [24] Mn [25,26] and Re, [27] Ru, Rh, Ir, [15,28,29] Os, [30] Co, [31] group 10: Ni, [32] Pd, [32,[33][34][35] Pt, [14,30,34] and group 11: [35] , and rare earth metals. [36,37] This could be due to the flexible nature of the ligand moieties, which adopt to several metallacyclic rings depending upon the coordination to the central metal atom.…”
Section: Introductionmentioning
confidence: 99%
“…132,7(t)o in I and 132. 3(2)0 in 1I-J. It is interesting that despite the electronic relationship of acetylacetone and II (which although not isoelectronic are closely related), although Group 10 complexes of acetylacetone all contain planar six-membered rings, here the rings are all puckered.…”
mentioning
confidence: 94%
“…Anionic functional ligands of this type are analogues of the more familiar β-diketonate ligands, most notably aceylacetonate (acac). [1][2][3][4] On the other hand, dichalcogenoimidodiphosphinato anions [R 2 P(X)NP(Y)R 2 ] − (R = R = Me, Pr, Ph; X Y O, S, Se) coordinate to the metals forming inorganic (carbon-free) chelate rings. Such chelates are widely used in metal extraction, catalytic, and medicinal applications.…”
Section: Introductionmentioning
confidence: 99%