Literature DB >> 21578102

Tricarbon-yl(η-flavone)chromium(0).

Johannes H van Tonder, Barend C B Bezuidenhoudt, J Marthinus Janse van Rensburg.   

Abstract

In the title compound, [Cr(C(15)H(10)O(2))(CO)(3)], the Cr(CO)(3) unit exhibits a three-legged piano-stool conformation. The chromium metal centre is coordinated by the phenyl ring of the flavone ligand [Cr-(phenyl centroid) distance = 1.709 (1) Å]. The ligand is approximately planar, the dihedral angles between the γ-pyrone ring and the phenyl ring and between the γ-pyrone and the phenyl-ene ring being 2.91 (5) and 3.90 (5)°, respectively. The mol-ecular packing shows π-π stacking between the flavone ligands of neighbouring mol-ecules.

Entities:  

Year:  2009        PMID: 21578102      PMCID: PMC2971426          DOI: 10.1107/S1600536809040525

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For the crystal structure of Cr(CO)3(C15H12O2), see: Dominique et al. (1999 ▶). For comparison bond distances, see: Allen (2002 ▶). For related structures, see: Zeller et al. (2004 ▶); Zhang et al. (2005 ▶); Czerwinski et al. (2003 ▶); Guzei & Czerwinski (2004 ▶). For the biological activity of flavonoids, see: Rice-Evans & Packer (2003 ▶).

Experimental

Crystal data

[Cr(C15H10O2)(CO)3] M = 358.26 Triclinic, a = 7.2853 (2) Å b = 9.6427 (3) Å c = 11.6466 (4) Å α = 78.545 (1)° β = 79.554 (1)° γ = 70.005 (1)° V = 747.81 (4) Å3 Z = 2 Mo Kα radiation μ = 0.79 mm−1 T = 173 K 0.45 × 0.32 × 0.19 mm

Data collection

Bruker APEXII CCD diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2004 ▶) T min = 0.717, T max = 0.864 8083 measured reflections 3600 independent reflections 3062 reflections with I > 2σ(I) R int = 0.022

Refinement

R[F 2 > 2σ(F 2)] = 0.037 wR(F 2) = 0.105 S = 1.06 3600 reflections 205 parameters H-atom parameters constrained Δρmax = 0.52 e Å−3 Δρmin = −0.55 e Å−3 Data collection: APEX2 (Bruker, 2005 ▶); cell refinement: SAINT-Plus (Bruker, 2004 ▶); data reduction: SAINT-Plus; program(s) used to solve structure: SIR97 (Altomare et al., 1999 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: DIAMOND (Brandenburg & Putz, 2005 ▶); software used to prepare material for publication: WinGX (Farrugia, 1999 ▶). Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809040525/ng2657sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536809040525/ng2657Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Cr(C15H10O2)(CO)3]Z = 2
Mr = 358.26F(000) = 364
Triclinic, P1Dx = 1.591 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 7.2853 (2) ÅCell parameters from 3694 reflections
b = 9.6427 (3) Åθ = 2.3–28.2°
c = 11.6466 (4) ŵ = 0.79 mm1
α = 78.545 (1)°T = 173 K
β = 79.554 (1)°Irregular, orange
γ = 70.005 (1)°0.45 × 0.32 × 0.19 mm
V = 747.81 (4) Å3
Bruker APEXII CCD diffractometer3600 independent reflections
Radiation source: fine-focus sealed tube3062 reflections with I > 2σ(I)
graphiteRint = 0.022
φ and ω scansθmax = 28°, θmin = 1.8°
Absorption correction: multi-scan (SADABS; Bruker, 2004)h = −9→8
Tmin = 0.717, Tmax = 0.864k = −12→12
8083 measured reflectionsl = −15→14
Refinement on F20 restraints
Least-squares matrix: fullH-atom parameters constrained
R[F2 > 2σ(F2)] = 0.037w = 1/[σ2(Fo2) + (0.0513P)2 + 0.3895P] where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.105(Δ/σ)max = 0.001
S = 1.06Δρmax = 0.52 e Å3
3600 reflectionsΔρmin = −0.55 e Å3
205 parameters
Experimental. The intensity data was collected on a Bruker Apex II CCD diffractometer using an exposure time of 10 s/frame. The 509 frames were collected with a frame width of 0.5° covering up to θ = 28° with 99.8% completeness accomplished.
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
xyzUiso*/Ueq
Cr0.44722 (4)0.35008 (3)0.85182 (3)0.02434 (11)
O50.6342 (2)0.24078 (16)0.52790 (12)0.0282 (3)
O41.1793 (2)0.29078 (17)0.44675 (15)0.0349 (4)
O30.2698 (2)0.3373 (2)1.10514 (14)0.0421 (4)
C20.6832 (3)0.3367 (2)0.57827 (16)0.0241 (4)
C30.8617 (3)0.3562 (2)0.55295 (18)0.0267 (4)
H30.88790.42470.5910.032*
C100.9548 (3)0.1789 (2)0.41199 (17)0.0249 (4)
C130.3382 (3)0.3412 (2)1.00763 (19)0.0292 (3)
O10.4968 (3)0.02553 (19)0.86574 (17)0.0499 (5)
C90.7671 (3)0.1667 (2)0.44291 (18)0.0273 (4)
C120.6912 (3)0.2990 (2)0.90154 (18)0.0292 (3)
O20.8445 (2)0.26801 (19)0.93196 (16)0.0425 (3)
C51.0793 (3)0.1028 (2)0.32237 (19)0.0311 (4)
H51.20830.10970.29990.037*
C2'0.5336 (3)0.5228 (2)0.72042 (18)0.0278 (4)
H2'0.6530.54610.70820.033*
C1'0.5171 (3)0.4148 (2)0.65939 (17)0.0257 (4)
C41.0145 (3)0.2762 (2)0.46978 (17)0.0255 (4)
C6'0.3370 (3)0.3817 (2)0.68058 (18)0.0306 (4)
H6'0.32260.30990.64060.037*
C110.4775 (3)0.1501 (2)0.86148 (18)0.02916 (17)
C3'0.3758 (3)0.5956 (2)0.79855 (19)0.0317 (5)
H3'0.38720.670.83690.038*
C80.7000 (4)0.0807 (2)0.3874 (2)0.0348 (5)
H80.57120.07330.40940.042*
C4'0.2009 (3)0.5587 (3)0.8202 (2)0.0354 (5)
H4'0.09640.60490.8760.042*
C5'0.1799 (3)0.4541 (3)0.7601 (2)0.0361 (5)
H5'0.05970.43190.77280.043*
C70.8262 (4)0.0070 (3)0.3002 (2)0.0398 (5)
H70.7839−0.05280.26170.048*
C61.0148 (4)0.0180 (2)0.2667 (2)0.0381 (5)
H61.099−0.03320.20550.046*
U11U22U33U12U13U23
Cr0.01993 (17)0.02901 (19)0.02080 (17)−0.00703 (13)−0.00249 (12)0.00247 (12)
O50.0261 (7)0.0341 (7)0.0279 (7)−0.0153 (6)−0.0025 (6)−0.0027 (6)
O40.0274 (8)0.0387 (8)0.0435 (9)−0.0175 (7)0.0046 (7)−0.0124 (7)
O30.0351 (9)0.0547 (10)0.0292 (8)−0.0129 (8)0.0047 (7)−0.0001 (7)
C20.0270 (10)0.0263 (9)0.0193 (9)−0.0107 (8)−0.0069 (8)0.0040 (7)
C30.0283 (10)0.0280 (10)0.0264 (10)−0.0130 (8)−0.0034 (8)−0.0029 (8)
C100.0284 (10)0.0215 (9)0.0242 (9)−0.0093 (8)−0.0069 (8)0.0033 (7)
C130.0240 (7)0.0315 (7)0.0279 (7)−0.0069 (6)−0.0014 (6)0.0000 (6)
O10.0698 (13)0.0385 (9)0.0470 (10)−0.0233 (9)−0.0162 (10)0.0000 (8)
C90.0333 (11)0.0253 (9)0.0247 (9)−0.0127 (8)−0.0075 (8)0.0030 (8)
C120.0240 (7)0.0315 (7)0.0279 (7)−0.0069 (6)−0.0014 (6)0.0000 (6)
O20.0299 (6)0.0450 (6)0.0502 (6)−0.0059 (7)−0.0131 (7)−0.0045 (8)
C50.0355 (11)0.0258 (10)0.0305 (10)−0.0085 (9)−0.0039 (9)−0.0034 (8)
C2'0.0260 (10)0.0272 (10)0.0264 (10)−0.0083 (8)−0.0029 (8)0.0044 (8)
C1'0.0222 (9)0.0312 (10)0.0199 (9)−0.0083 (8)−0.0037 (7)0.0052 (7)
C40.0284 (10)0.0241 (9)0.0244 (9)−0.0116 (8)−0.0020 (8)0.0001 (7)
C6'0.0258 (10)0.0405 (12)0.0239 (10)−0.0111 (9)−0.0070 (8)0.0036 (8)
C110.0240 (2)0.03146 (19)0.02793 (16)−0.0069 (6)−0.0014 (6)0.0000 (6)
C3'0.0316 (11)0.0271 (10)0.0284 (10)−0.0026 (8)−0.0039 (9)0.0022 (8)
C80.0392 (12)0.0337 (11)0.0379 (12)−0.0180 (10)−0.0123 (10)−0.0014 (9)
C4'0.0249 (11)0.0385 (12)0.0302 (11)0.0005 (9)−0.0026 (9)0.0039 (9)
C5'0.0190 (10)0.0506 (13)0.0312 (11)−0.0079 (9)−0.0061 (8)0.0081 (10)
C70.0534 (15)0.0326 (11)0.0410 (13)−0.0176 (11)−0.0167 (11)−0.0055 (10)
C60.0457 (14)0.0303 (11)0.0368 (12)−0.0072 (10)−0.0060 (10)−0.0095 (9)
Cr—C131.842 (2)C9—C81.396 (3)
Cr—C121.844 (2)C12—O21.155 (3)
Cr—C111.847 (2)C5—C61.376 (3)
Cr—C2'2.206 (2)C5—H50.95
Cr—C4'2.209 (2)C2'—C3'1.402 (3)
Cr—C6'2.211 (2)C2'—C1'1.420 (3)
Cr—C1'2.2180 (19)C2'—H2'0.95
Cr—C5'2.221 (2)C1'—C6'1.422 (3)
Cr—C3'2.225 (2)C6'—C5'1.407 (3)
O5—C21.358 (2)C6'—H6'0.95
O5—C91.374 (3)C3'—C4'1.404 (3)
O4—C41.232 (2)C3'—H3'0.95
O3—C131.153 (3)C8—C71.373 (3)
C2—C31.349 (3)C8—H80.95
C2—C1'1.473 (3)C4'—C5'1.399 (3)
C3—C41.446 (3)C4'—H4'0.95
C3—H30.95C5'—H5'0.95
C10—C91.388 (3)C7—C61.393 (4)
C10—C51.399 (3)C7—H70.95
C10—C41.469 (3)C6—H60.95
O1—C111.153 (3)
C13—Cr—C1288.71 (9)C6—C5—H5120
C13—Cr—C1188.80 (9)C10—C5—H5120
C12—Cr—C1189.60 (9)C3'—C2'—C1'120.78 (19)
C13—Cr—C2'134.26 (9)C3'—C2'—Cr72.30 (12)
C12—Cr—C2'86.71 (8)C1'—C2'—Cr71.73 (11)
C11—Cr—C2'136.58 (9)C3'—C2'—H2'119.6
C13—Cr—C4'85.97 (9)C1'—C2'—H2'119.6
C12—Cr—C4'135.57 (9)Cr—C2'—H2'128.7
C11—Cr—C4'134.24 (9)C2'—C1'—C6'118.15 (19)
C2'—Cr—C4'66.83 (8)C2'—C1'—C2121.01 (18)
C13—Cr—C6'135.41 (9)C6'—C1'—C2120.83 (18)
C12—Cr—C6'135.54 (9)C2'—C1'—Cr70.84 (11)
C11—Cr—C6'86.67 (9)C6'—C1'—Cr70.99 (11)
C2'—Cr—C6'67.00 (8)C2—C1'—Cr128.43 (13)
C4'—Cr—C6'66.69 (9)O4—C4—C3123.10 (18)
C13—Cr—C1'165.52 (8)O4—C4—C10122.58 (19)
C12—Cr—C1'101.05 (8)C3—C4—C10114.29 (17)
C11—Cr—C1'101.82 (8)C5'—C6'—C1'120.8 (2)
C2'—Cr—C1'37.43 (8)C5'—C6'—Cr71.90 (12)
C4'—Cr—C1'79.57 (8)C1'—C6'—Cr71.55 (11)
C6'—Cr—C1'37.46 (7)C5'—C6'—H6'119.6
C13—Cr—C5'101.29 (9)C1'—C6'—H6'119.6
C12—Cr—C5'165.57 (9)Cr—C6'—H6'129.4
C11—Cr—C5'100.88 (9)O1—C11—Cr179.00 (19)
C2'—Cr—C5'78.86 (8)C2'—C3'—C4'120.1 (2)
C4'—Cr—C5'36.82 (9)C2'—C3'—Cr70.83 (12)
C6'—Cr—C5'37.02 (8)C4'—C3'—Cr70.90 (12)
C1'—Cr—C5'67.29 (8)C2'—C3'—H3'119.9
C13—Cr—C3'100.70 (9)C4'—C3'—H3'119.9
C12—Cr—C3'101.88 (9)Cr—C3'—H3'131
C11—Cr—C3'165.16 (9)C7—C8—C9117.8 (2)
C2'—Cr—C3'36.87 (8)C7—C8—H8121.1
C4'—Cr—C3'36.92 (8)C9—C8—H8121.1
C6'—Cr—C3'78.55 (8)C5'—C4'—C3'120.2 (2)
C1'—Cr—C3'67.01 (8)C5'—C4'—Cr72.06 (13)
C5'—Cr—C3'66.27 (9)C3'—C4'—Cr72.17 (12)
C2—O5—C9118.91 (15)C5'—C4'—H4'119.9
C3—C2—O5122.59 (18)C3'—C4'—H4'119.9
C3—C2—C1'126.27 (18)Cr—C4'—H4'128
O5—C2—C1'111.14 (16)C4'—C5'—C6'119.9 (2)
C2—C3—C4122.13 (18)C4'—C5'—Cr71.11 (12)
C2—C3—H3118.9C6'—C5'—Cr71.08 (11)
C4—C3—H3118.9C4'—C5'—H5'120
C9—C10—C5118.77 (19)C6'—C5'—H5'120
C9—C10—C4119.53 (19)Cr—C5'—H5'130.3
C5—C10—C4121.63 (18)C8—C7—C6121.5 (2)
O3—C13—Cr179.21 (19)C8—C7—H7119.2
O5—C9—C10122.38 (17)C6—C7—H7119.2
O5—C9—C8115.70 (19)C5—C6—C7120.0 (2)
C10—C9—C8121.9 (2)C5—C6—H6120
O2—C12—Cr179.4 (2)C7—C6—H6120
C6—C5—C10119.9 (2)
C9—O5—C2—C3−3.8 (3)C11—Cr—C6'—C5'113.02 (14)
C9—O5—C2—C1'175.14 (15)C2'—Cr—C6'—C5'−102.38 (15)
O5—C2—C3—C40.1 (3)C4'—Cr—C6'—C5'−28.79 (13)
C1'—C2—C3—C4−178.63 (17)C1'—Cr—C6'—C5'−132.57 (19)
C2—O5—C9—C104.3 (3)C3'—Cr—C6'—C5'−65.58 (14)
C2—O5—C9—C8−174.35 (17)C13—Cr—C6'—C1'160.68 (13)
C5—C10—C9—O5−178.36 (17)C12—Cr—C6'—C1'−28.37 (18)
C4—C10—C9—O5−1.2 (3)C11—Cr—C6'—C1'−114.41 (13)
C5—C10—C9—C80.2 (3)C2'—Cr—C6'—C1'30.19 (12)
C4—C10—C9—C8177.37 (18)C4'—Cr—C6'—C1'103.78 (14)
C9—C10—C5—C60.0 (3)C5'—Cr—C6'—C1'132.57 (19)
C4—C10—C5—C6−177.10 (19)C3'—Cr—C6'—C1'66.99 (13)
C13—Cr—C2'—C3'−29.87 (18)C1'—C2'—C3'—C4'2.1 (3)
C12—Cr—C2'—C3'−114.84 (14)Cr—C2'—C3'—C4'−52.98 (17)
C11—Cr—C2'—C3'159.22 (14)C1'—C2'—C3'—Cr55.03 (16)
C4'—Cr—C2'—C3'28.54 (13)C13—Cr—C3'—C2'158.72 (13)
C6'—Cr—C2'—C3'101.93 (14)C12—Cr—C3'—C2'67.79 (14)
C1'—Cr—C2'—C3'132.14 (18)C11—Cr—C3'—C2'−72.2 (4)
C5'—Cr—C2'—C3'65.10 (13)C4'—Cr—C3'—C2'−133.0 (2)
C13—Cr—C2'—C1'−162.01 (13)C6'—Cr—C3'—C2'−66.76 (13)
C12—Cr—C2'—C1'113.01 (13)C1'—Cr—C3'—C2'−29.31 (12)
C11—Cr—C2'—C1'27.07 (17)C5'—Cr—C3'—C2'−103.55 (14)
C4'—Cr—C2'—C1'−103.61 (13)C13—Cr—C3'—C4'−68.25 (15)
C6'—Cr—C2'—C1'−30.22 (12)C12—Cr—C3'—C4'−159.19 (14)
C5'—Cr—C2'—C1'−67.04 (12)C11—Cr—C3'—C4'60.8 (4)
C3'—Cr—C2'—C1'−132.14 (18)C2'—Cr—C3'—C4'133.0 (2)
C3'—C2'—C1'—C6'−0.5 (3)C6'—Cr—C3'—C4'66.26 (13)
Cr—C2'—C1'—C6'54.75 (15)C1'—Cr—C3'—C4'103.72 (14)
C3'—C2'—C1'—C2−179.27 (17)C5'—Cr—C3'—C4'29.48 (13)
Cr—C2'—C1'—C2−123.97 (17)O5—C9—C8—C7178.69 (19)
C3'—C2'—C1'—Cr−55.30 (17)C10—C9—C8—C70.0 (3)
C3—C2—C1'—C2'0.1 (3)C2'—C3'—C4'—C5'−2.9 (3)
O5—C2—C1'—C2'−178.79 (16)Cr—C3'—C4'—C5'−55.84 (18)
C3—C2—C1'—C6'−178.62 (18)C2'—C3'—C4'—Cr52.95 (17)
O5—C2—C1'—C6'2.5 (2)C13—Cr—C4'—C5'−114.93 (14)
C3—C2—C1'—Cr−89.2 (2)C12—Cr—C4'—C5'161.05 (14)
O5—C2—C1'—Cr91.89 (19)C11—Cr—C4'—C5'−30.55 (19)
C13—Cr—C1'—C2'62.2 (4)C2'—Cr—C4'—C5'102.77 (14)
C12—Cr—C1'—C2'−69.43 (13)C6'—Cr—C4'—C5'28.94 (13)
C11—Cr—C1'—C2'−161.36 (12)C1'—Cr—C4'—C5'65.85 (13)
C4'—Cr—C1'—C2'65.30 (12)C3'—Cr—C4'—C5'131.3 (2)
C6'—Cr—C1'—C2'130.39 (18)C13—Cr—C4'—C3'113.80 (14)
C5'—Cr—C1'—C2'101.66 (14)C12—Cr—C4'—C3'29.78 (19)
C3'—Cr—C1'—C2'28.90 (12)C11—Cr—C4'—C3'−161.82 (14)
C13—Cr—C1'—C6'−68.2 (4)C2'—Cr—C4'—C3'−28.50 (13)
C12—Cr—C1'—C6'160.18 (13)C6'—Cr—C4'—C3'−102.33 (14)
C11—Cr—C1'—C6'68.24 (14)C1'—Cr—C4'—C3'−65.42 (13)
C2'—Cr—C1'—C6'−130.39 (18)C5'—Cr—C4'—C3'−131.3 (2)
C4'—Cr—C1'—C6'−65.09 (13)C3'—C4'—C5'—C6'2.2 (3)
C5'—Cr—C1'—C6'−28.73 (13)Cr—C4'—C5'—C6'−53.67 (18)
C3'—Cr—C1'—C6'−101.49 (14)C3'—C4'—C5'—Cr55.89 (17)
C13—Cr—C1'—C2177.0 (3)C1'—C6'—C5'—C4'−0.7 (3)
C12—Cr—C1'—C245.44 (19)Cr—C6'—C5'—C4'53.69 (18)
C11—Cr—C1'—C2−46.49 (19)C1'—C6'—C5'—Cr−54.40 (17)
C2'—Cr—C1'—C2114.9 (2)C13—Cr—C5'—C4'67.28 (14)
C4'—Cr—C1'—C2−179.83 (19)C12—Cr—C5'—C4'−65.8 (4)
C6'—Cr—C1'—C2−114.7 (2)C11—Cr—C5'—C4'158.24 (14)
C5'—Cr—C1'—C2−143.5 (2)C2'—Cr—C5'—C4'−66.03 (13)
C3'—Cr—C1'—C2143.77 (19)C6'—Cr—C5'—C4'−132.4 (2)
C2—C3—C4—O4−178.92 (19)C1'—Cr—C5'—C4'−103.38 (14)
C2—C3—C4—C102.9 (3)C3'—Cr—C5'—C4'−29.55 (13)
C9—C10—C4—O4179.48 (18)C13—Cr—C5'—C6'−160.28 (13)
C5—C10—C4—O4−3.4 (3)C12—Cr—C5'—C6'66.6 (4)
C9—C10—C4—C3−2.3 (3)C11—Cr—C5'—C6'−69.33 (14)
C5—C10—C4—C3174.81 (18)C2'—Cr—C5'—C6'66.40 (13)
C2'—C1'—C6'—C5'−0.1 (3)C4'—Cr—C5'—C6'132.4 (2)
C2—C1'—C6'—C5'178.61 (18)C1'—Cr—C5'—C6'29.05 (12)
Cr—C1'—C6'—C5'54.56 (17)C3'—Cr—C5'—C6'102.88 (14)
C2'—C1'—C6'—Cr−54.68 (16)C9—C8—C7—C6−0.5 (3)
C2—C1'—C6'—Cr124.05 (17)C10—C5—C6—C7−0.4 (3)
C13—Cr—C6'—C5'28.11 (19)C8—C7—C6—C50.7 (4)
C12—Cr—C6'—C5'−160.94 (14)
  4 in total

1.  The Cambridge Structural Database: a quarter of a million crystal structures and rising.

Authors:  Frank H Allen
Journal:  Acta Crystallogr B       Date:  2002-05-29

2.  (eta6-2-Bromo-1,1'-biphenyl)-tricarbonylchromium.

Authors:  Curtis J Czerwinski; Ilia A Guzei; Tanya J Cordes; Kevin M Czerwinski; Nevin A Mlodik
Journal:  Acta Crystallogr C       Date:  2003-11-08       Impact factor: 1.172

3.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

4.  (eta6-Biphenyl)tricarbonylchromium and mu-(eta6:eta6)-biphenyl-bis(tricarbonylchromium).

Authors:  Ilia A Guzei; Curtis J Czerwinski
Journal:  Acta Crystallogr C       Date:  2004-11-11       Impact factor: 1.172

  4 in total
  3 in total

1.  Racemic tricarbon-yl(η-7-meth-oxy-flavan)chromium(0).

Authors:  Johannes H van Tonder; Barend C B Bezuidenhoudt; J Marthinus Janse van Rensburg
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-07-10

2.  Racemic tricarbonyl[(4a,5,6,7,8,8a-η)-2-phenyl-3,4-dihydro-2H-1-benzopyran]chromium(0).

Authors:  Johannes H van Tonder; Barend C B Bezuidenhoudt; J Marthinus Janse van Rensburg
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-08-11

3.  Racemic tricarbon-yl[7-meth-oxy-2-(η-phen-yl)chromane]-chromium(0).

Authors:  Mukut Gohain; Theunis J Muller; Barend C B Bezuidenhoudt
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-03-12
  3 in total

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