Crystal structure of β-d,l-psicose.

The title compound, C6H12O6, a C-3 position epimer of fructose, was crystallized from an aqueous solution of equimolar mixture of d- and l-psicose (1,3,4,5,6-penta-hydroxy-hexan-2-one, ribo-2-hexulose, allulose), and it was confirmed that d-psicose (or l-psicose) formed β-pyran-ose with a (2) C 5 (or (5) C 2) conformation. In the crystal, an O-H⋯O hydrogen bond between the hy-droxy groups at the C-3 and C-2 positions connects homochiral mol-ecules into a column along the b axis. The columns are linked by other O-H⋯O hydrogen bonds between d- and l-psicose mol-ecules, forming a three-dimensional network. An intra-molecular O-H⋯O hydrogen bond is also observed. The cell volume of racemic β-d,l-psicose [763.21 (6) Å(3)] is almost the same as that of chiral β-d-psicose [753.06 Å(3)].

Related literature

For the crystal structure of the chiral β-d-psicose, see: Kwiecien et al. (2008 ▸); Fukada et al. (2010 ▸). For the synthesis of the chiral d-psicose, see: Itoh et al. (1995 ▸); Takeshita et al. (2000 ▸). For the synthesis of the chiral l-psicose, see: Takeshita et al. (1996 ▸).

Experimental

Crystal data

C6H12O6

M = 180.16

Orthorhombic,

a = 11.2629 (5) Å

b = 5.3552 (3) Å

c = 12.6538 (6) Å

V = 763.21 (6) Å3

Z = 4

Cu Kα radiation

μ = 1.25 mm−1

T = 296 K

0.10 × 0.10 × 0.10 mm

Data collection

Rigaku R-AXIS RAPID diffractometer

Absorption correction: multi-scan (ABSCOR; Higashi, 1995 ▸) T min = 0.442, T max = 0.883

12119 measured reflections

1400 independent reflections

1295 reflections with F 2 > 2σ(F 2)

R int = 0.139

Refinement

R[F 2 > 2σ(F 2)] = 0.048

wR(F 2) = 0.102

S = 1.04

1400 reflections

116 parameters

1 restraint

H-atom parameters constrained

Δρmax = 0.25 e Å−3

Δρmin = −0.23 e Å−3

Absolute structure: Flack (1983 ▸), 666 Friedel pairs

Absolute structure parameter: 0.1 (4)

Data collection: RAPID-AUTO (Rigaku, 2009 ▸); cell refinement: RAPID-AUTO; data reduction: RAPID-AUTO; program(s) used to solve structure: SIR2011 (Burla et al., 2012 ▸); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2015 ▸); molecular graphics: CrystalStructure (Rigaku, 2014 ▸); software used to prepare material for publication: CrystalStructure.

Crystal structure: contains datablock(s) global, I. DOI: 10.1107/S2056989015006623/is5394sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989015006623/is5394Isup2.hkl

Click here for additional data file.

ORTEP . DOI: 10.1107/S2056989015006623/is5394fig1.tif

ORTEP view of the title compound with the atom-labeling scheme. The thermal ellipsoids of all non-hydrogen atoms are drawn at the 50% probability level. H atoms are shown as small spheres of arbitrary radius.

Click here for additional data file.

b . DOI: 10.1107/S2056989015006623/is5394fig2.tif

Part of the crystal structure of the title compound with hydrogen-bonding network represented as green solid lines, viewed down the b-axis. The hydrogen atoms are omitted for clarity.

Click here for additional data file.

d et al. . DOI: 10.1107/S2056989015006623/is5394fig3.tif

Part of the crystal structure of the chiral β-d-psicose (Fukada et al., 2010) with hydrogen-bonding network represented as green solid lines. The hydrogen atoms are omitted for clarity.

CCDC reference: 1057484

Additional supporting information: crystallographic information; 3D view; checkCIF report

C6H12O6	Dx = 1.568 Mg m−3
Mr = 180.16	Cu Kα radiation, λ = 1.54187 Å
Orthorhombic, Pna21	Cell parameters from 5584 reflections
a = 11.2629 (5) Å	θ = 3.5–68.5°
b = 5.3552 (3) Å	µ = 1.25 mm−1
c = 12.6538 (6) Å	T = 296 K
V = 763.21 (6) Å3	Block, colorless
Z = 4	0.10 × 0.10 × 0.10 mm
F(000) = 384.00

Rigaku R-AXIS RAPID diffractometer	1295 reflections with F2 > 2σ(F2)
Detector resolution: 10.000 pixels mm-1	Rint = 0.139
ω scans	θmax = 68.2°, θmin = 7.0°
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	h = −13→13
Tmin = 0.442, Tmax = 0.883	k = −6→6
12119 measured reflections	l = −15→15
1400 independent reflections

Refinement on F2	H-atom parameters constrained
R[F2 > 2σ(F2)] = 0.048	w = 1/[σ2(Fo2) + (0.0359P)2] where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.102	(Δ/σ)max < 0.001
S = 1.04	Δρmax = 0.25 e Å−3
1400 reflections	Δρmin = −0.23 e Å−3
116 parameters	Extinction correction: SHELXL
1 restraint	Extinction coefficient: 0.039 (3)
Primary atom site location: structure-invariant direct methods	Absolute structure: Flack (1983), 666 Friedel pairs
Secondary atom site location: difference Fourier map	Absolute structure parameter: 0.1 (4)
Hydrogen site location: inferred from neighbouring sites

Geometry. ENTER SPECIAL DETAILS OF THE MOLECULAR GEOMETRY

Refinement. Refinement was performed using all reflections. The weighted R-factor (wR) and goodness of fit (S) are based on F2. R-factor (gt) are based on F. The threshold expression of F2 > 2.0 σ(F2) is used only for calculating R-factor (gt).

	x	y	z	Uiso*/Ueq
O1	0.6428 (2)	1.0475 (5)	0.0101 (2)	0.0321 (7)
O2	0.8138 (2)	1.3225 (4)	0.1244 (2)	0.0283 (6)
O3	0.9712 (2)	0.7407 (4)	0.0986 (2)	0.0278 (6)
O4	1.12635 (19)	0.9941 (5)	0.2360 (2)	0.0306 (7)
O5	0.9520 (3)	0.6941 (5)	0.3201 (2)	0.0368 (7)
O6	0.75926 (19)	0.9487 (5)	0.2068 (2)	0.0243 (6)
C1	0.7610 (3)	0.9600 (8)	0.0218 (3)	0.0275 (8)
C2	0.8199 (3)	1.0614 (6)	0.1199 (3)	0.0211 (7)
C3	0.9525 (3)	0.9956 (6)	0.1238 (3)	0.0223 (7)
C4	1.0049 (3)	1.0665 (7)	0.2306 (2)	0.0233 (8)
C5	0.9337 (3)	0.9564 (7)	0.3210 (3)	0.0266 (8)
C6	0.8044 (3)	1.0258 (7)	0.3083 (3)	0.0289 (8)
H1B	0.80695	1.00892	−0.03968	0.0330*
H1C	0.76042	0.77904	0.02497	0.0330*
H1A	0.59772	0.95756	0.04384	0.0386*
H2A	0.75043	1.36467	0.15074	0.0340*
H3A	0.92832	0.65324	0.13561	0.0333*
H3B	0.99273	1.0959	0.06985	0.0268*
H4B	1.00147	1.24872	0.23691	0.0280*
H4A	1.1313	0.84167	0.23198	0.0367*
H5A	0.92192	0.63218	0.37294	0.0442*
H5B	0.96322	1.0246	0.38792	0.0319*
H6A	0.75828	0.94707	0.36378	0.0347*
H6B	0.79566	1.20525	0.31544	0.0347*

	U11	U22	U33	U12	U13	U23
O1	0.0232 (14)	0.0431 (18)	0.0301 (13)	−0.0019 (11)	−0.0058 (11)	0.0126 (12)
O2	0.0238 (12)	0.0228 (13)	0.0384 (14)	0.0010 (9)	0.0057 (11)	0.0025 (13)
O3	0.0252 (12)	0.0240 (13)	0.0340 (14)	0.0013 (10)	0.0068 (10)	−0.0020 (11)
O4	0.0193 (12)	0.0265 (14)	0.0459 (17)	0.0004 (10)	−0.0022 (10)	0.0013 (12)
O5	0.0475 (17)	0.0309 (15)	0.0322 (15)	0.0064 (12)	0.0101 (11)	0.0101 (12)
O6	0.0230 (12)	0.0297 (14)	0.0203 (11)	−0.0057 (10)	0.0027 (10)	0.0002 (12)
C1	0.025 (2)	0.032 (2)	0.0254 (19)	−0.0001 (15)	−0.0001 (14)	0.0024 (18)
C2	0.0211 (17)	0.0228 (17)	0.0195 (16)	0.0012 (12)	0.0034 (14)	0.0043 (16)
C3	0.0197 (19)	0.0233 (17)	0.0239 (17)	0.0009 (12)	0.0038 (14)	0.0042 (14)
C4	0.0189 (17)	0.025 (2)	0.0265 (19)	0.0009 (13)	0.0000 (13)	0.0006 (15)
C5	0.030 (2)	0.030 (2)	0.0201 (17)	0.0027 (14)	−0.0011 (15)	−0.0001 (15)
C6	0.0272 (18)	0.039 (2)	0.0209 (17)	0.0006 (15)	0.0055 (15)	−0.0002 (15)

O1—C1	1.419 (4)	O1—H1A	0.820
O2—C2	1.401 (4)	O2—H2A	0.820
O3—C3	1.418 (4)	O3—H3A	0.820
O4—C4	1.423 (4)	O4—H4A	0.820
O5—C5	1.419 (4)	O5—H5A	0.820
O6—C2	1.428 (4)	C1—H1B	0.970
O6—C6	1.442 (4)	C1—H1C	0.970
C1—C2	1.509 (5)	C3—H3B	0.980
C2—C3	1.535 (5)	C4—H4B	0.980
C3—C4	1.523 (5)	C5—H5B	0.980
C4—C5	1.516 (5)	C6—H6A	0.970
C5—C6	1.512 (5)	C6—H6B	0.970
C2—O6—C6	113.3 (2)	C4—O4—H4A	109.469
O1—C1—C2	112.3 (3)	C5—O5—H5A	109.469
O2—C2—O6	111.6 (3)	O1—C1—H1B	109.152
O2—C2—C1	111.8 (3)	O1—C1—H1C	109.152
O2—C2—C3	106.0 (3)	C2—C1—H1B	109.145
O6—C2—C1	105.7 (3)	C2—C1—H1C	109.145
O6—C2—C3	110.1 (3)	H1B—C1—H1C	107.867
C1—C2—C3	111.8 (3)	O3—C3—H3B	107.581
O3—C3—C2	111.0 (3)	C2—C3—H3B	107.578
O3—C3—C4	112.5 (3)	C4—C3—H3B	107.580
C2—C3—C4	110.4 (3)	O4—C4—H4B	107.757
O4—C4—C3	110.3 (3)	C3—C4—H4B	107.761
O4—C4—C5	111.5 (3)	C5—C4—H4B	107.767
C3—C4—C5	111.6 (3)	O5—C5—H5B	109.099
O5—C5—C4	107.5 (3)	C4—C5—H5B	109.103
O5—C5—C6	112.5 (3)	C6—C5—H5B	109.093
C4—C5—C6	109.5 (3)	O6—C6—H6A	109.357
O6—C6—C5	111.4 (3)	O6—C6—H6B	109.357
C1—O1—H1A	109.471	C5—C6—H6A	109.358
C2—O2—H2A	109.471	C5—C6—H6B	109.358
C3—O3—H3A	109.470	H6A—C6—H6B	107.992
C2—O6—C6—C5	−60.7 (3)	C1—C2—C3—C4	−171.7 (2)
C6—O6—C2—O2	−58.2 (3)	O3—C3—C4—O4	52.5 (3)
C6—O6—C2—C1	−179.9 (2)	O3—C3—C4—C5	−72.0 (3)
C6—O6—C2—C3	59.2 (3)	C2—C3—C4—O4	177.1 (2)
O1—C1—C2—O2	−53.5 (4)	C2—C3—C4—C5	52.6 (3)
O1—C1—C2—O6	68.1 (3)	O4—C4—C5—O5	−54.2 (3)
O1—C1—C2—C3	−172.1 (2)	O4—C4—C5—C6	−176.7 (2)
O2—C2—C3—O3	−168.2 (2)	C3—C4—C5—O5	69.6 (3)
O2—C2—C3—C4	66.4 (3)	C3—C4—C5—C6	−52.9 (3)
O6—C2—C3—O3	71.0 (3)	O5—C5—C6—O6	−63.8 (4)
O6—C2—C3—C4	−54.4 (3)	C4—C5—C6—O6	55.7 (4)
C1—C2—C3—O3	−46.2 (4)

D—H···A	D—H	H···A	D···A	D—H···A
O1—H1A···O3i	0.82	1.91	2.715 (3)	168
O2—H2A···O4ii	0.82	1.92	2.724 (3)	166
O3—H3A···O2iii	0.82	2.20	2.874 (3)	140
O3—H3A···O5	0.82	2.36	2.822 (4)	117
O4—H4A···O6iv	0.82	2.14	2.829 (3)	141
O5—H5A···O1v	0.82	1.94	2.746 (4)	169

Table 1

Hydrogen-bond geometry (, )

DHA	DH	HA	D A	DHA
O1H1AO3i	0.82	1.91	2.715(3)	168
O2H2AO4ii	0.82	1.92	2.724(3)	166
O3H3AO2iii	0.82	2.20	2.874(3)	140
O3H3AO5	0.82	2.36	2.822(4)	117
O4H4AO6iv	0.82	2.14	2.829(3)	141
O5H5AO1v	0.82	1.94	2.746(4)	169

Symmetry codes: (i) ; (ii) ; (iii) ; (iv) ; (v) .