1974
DOI: 10.1107/s0567740874005140
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(−)589-[l-N,N,N',N'-tetrakis(2'-aminoethyl)-1,2-diaminopropane]cobalt(III) hexacyanocobaltate(III) trihydrate

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Cited by 11 publications
(9 citation statements)
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“…24,25 The violet fractions collected were combined, evaporated to dryness at 40 °C and recrystallized from chloroform/pentane, yielding 174 mg (90%). 1 H NMR (CDCl3, 300 MHz): δ 10.14 (d, 2H, 3 J ) 5.5 Hz), 7.96 (d, 2H, 3 J ) 7.6 Hz), 7.82 (t, 2H, 3 J ) 7.4 Hz), 7.74 (s, 2H), 7.52 (t, 2H, 3 J ) 5.8 Hz), 7.05 (t, 1H, 3 J ) 7.6 Hz), 6.88 (s, 2H), 6.84 (d, 2H, 3 J ) 7.7 Hz), 5.84 (s, 1H), 3.50 (dm, 2H, 2 J ) 15.6 Hz), 3.33 (br s, 2H), 2.93 (dd, 2H, 2 J ) 15.8 Hz, 3 J ) 6.6 Hz), 2.25 (dd, 2H, 3 J ) 5. 4 Hz, 4 J ) 5.4 Hz), 2.08 (td, 2H, 3 J ) 5.9 Hz, 2 J ) 10.1 Hz), 2.02 (td, 2H, 3 J ) 5.9 Hz, 3 J ) 1.8 Hz), 1.17 (s, 3H), 0.87 (d, 2H, 2 J ) 9.8 Hz), 0.42 (s, 3H).…”
Section: Methodsmentioning
confidence: 99%
See 2 more Smart Citations
“…24,25 The violet fractions collected were combined, evaporated to dryness at 40 °C and recrystallized from chloroform/pentane, yielding 174 mg (90%). 1 H NMR (CDCl3, 300 MHz): δ 10.14 (d, 2H, 3 J ) 5.5 Hz), 7.96 (d, 2H, 3 J ) 7.6 Hz), 7.82 (t, 2H, 3 J ) 7.4 Hz), 7.74 (s, 2H), 7.52 (t, 2H, 3 J ) 5.8 Hz), 7.05 (t, 1H, 3 J ) 7.6 Hz), 6.88 (s, 2H), 6.84 (d, 2H, 3 J ) 7.7 Hz), 5.84 (s, 1H), 3.50 (dm, 2H, 2 J ) 15.6 Hz), 3.33 (br s, 2H), 2.93 (dd, 2H, 2 J ) 15.8 Hz, 3 J ) 6.6 Hz), 2.25 (dd, 2H, 3 J ) 5. 4 Hz, 4 J ) 5.4 Hz), 2.08 (td, 2H, 3 J ) 5.9 Hz, 2 J ) 10.1 Hz), 2.02 (td, 2H, 3 J ) 5.9 Hz, 3 J ) 1.8 Hz), 1.17 (s, 3H), 0.87 (d, 2H, 2 J ) 9.8 Hz), 0.42 (s, 3H).…”
Section: Methodsmentioning
confidence: 99%
“…Predetermination of chirality at an octrahedrally coordinated metal center (OC-6) has been achieved through various methods. For example, in the hexadentate ligand “mepenten” the configuration at the stereogenic center determines unambiguously the helical chirality at the metal center. , An R configuration at C(2) induces the configuration Δ 2 Λ in the octahedral coordination sphere. In the case of several pentadentate ligands, the chirality at the metal center is predetermined by the configuration of the ligand too. , We were interested to achieve chiral predetermination with tetradendate ligands in OC-6 complexes, so that the remaining two sites can be occupied by either two monodentate ligands or one bidentate ligand.…”
Section: Introductionmentioning
confidence: 99%
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“…In the case of hexadentate ligands, e.g. ( R )- N , N , N ‘, N ‘-Tetrakis(2-aminoethyl)-1,2-propanediamine or analogs thereof, , the complex is coordinatively saturated, whereas in the case of a pentadentate ligand, e.g. ( R,R )-alamp or ( R,R )-promp, , one coordination site can be occupied by an additional monodentate ligand.…”
Section: Introductionmentioning
confidence: 99%
“…All the eight compounds containing hexacyanometallate ions and octahedral complexes with polyamine ligands that we were able to find in the literature (only compounds with five-membered ethylenediamine bridges were considered) incorporated similar associates. [2][3][4][5][6][7][8][9] Because the [M(CN) 6 ][M'(NR) 6 ] 6 associate is present in crystal structures irrespective of the composition and stoichiometry of compounds, it should be regarded as a structure-forming unit in compounds of this type.…”
mentioning
confidence: 99%