Literature DB >> 21581423

Low-temperature redetermination of 4-chloro-2-[tris-(hydroxy-meth-yl)methyl-imino-meth-yl]phenol as zwitterionic 4-chloro-2-[tris-(hydroxy-meth-yl)methyl-iminiometh-yl]phenolate.

Seik Weng Ng1.   

Abstract

The title Schiff base, C(11)H(14)ClNO(4), originally refined as a neutral mol-ecule [Chumakov, Antosyak, Mazus, Tsapkov & Samus (2000), Crystallogr. Rep.45, 945-950], is inter-preted as a zwitterionic compound. There are two independent zwitterions in the asymmetric unit. Five of the six hydr-oxy groups of the -CH(2)OH fragments are disordered. In one zwitterion, two are disordered over three sites [0.53 (1):0.33 (1):0.14 (1) and 0.65 (1):0.18 (1):0.17 (1)] and the third over two sites [0.66 (1):0.34 (1)]. In the second zwitterion, two are disordered over two sites [0.84 (1):0.16 (1) and 0.83 (1):0.17 (1)] and the third hydr-oxy group is ordered.

Entities:  

Year:  2008        PMID: 21581423      PMCID: PMC2960041          DOI: 10.1107/S160053680803866X

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


Related literature

The room-temperature crystal structure was inter­preted as a neutral mol­ecule; the disordered structure (the disorder confined to the hydr­oxy part of one of the six –CH2OH groups) refined to 0.072, see: Chumakov et al. (2000 ▶). The unsubstituted parent Schiff base is also a zwitterion; its structure has been determined several times, see: Asgedom et al. (1996 ▶); Odabas˛ogˇlu et al. (2003 ▶); Tatar et al. (2005 ▶); Zhang et al. (2000 ▶).

Experimental

Crystal data

C11H14ClNO4 M = 259.68 Triclinic, a = 7.0174 (1) Å b = 10.1935 (1) Å c = 16.7234 (2) Å α = 79.520 (1)° β = 89.031 (1)° γ = 85.258 (1)° V = 1172.27 (2) Å3 Z = 4 Mo Kα radiation μ = 0.33 mm−1 T = 100 (2) K 0.30 × 0.20 × 0.05 mm

Data collection

Bruker SMART APEX diffractometer Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ▶) T min = 0.908, T max = 0.984 11241 measured reflections 5361 independent reflections 4771 reflections with I > 2σ(I) R int = 0.018

Refinement

R[F 2 > 2σ(F 2)] = 0.042 wR(F 2) = 0.117 S = 1.01 5361 reflections 360 parameters 47 restraints H atoms treated by a mixture of independent and constrained refinement Δρmax = 0.41 e Å−3 Δρmin = −0.74 e Å−3 Data collection: APEX2 (Bruker, 2007 ▶); cell refinement: SAINT (Bruker, 2007 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: X-SEED (Barbour, 2001 ▶); software used to prepare material for publication: publCIF (Westrip, 2008 ▶). Crystal structure: contains datablocks global, I. DOI: 10.1107/S160053680803866X/tk2330sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S160053680803866X/tk2330Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C11H14ClNO4Z = 4
Mr = 259.68F000 = 544
Triclinic, P1Dx = 1.471 Mg m3
Hall symbol: -P 1Mo Kα radiation λ = 0.71073 Å
a = 7.0174 (1) ÅCell parameters from 6864 reflections
b = 10.1935 (1) Åθ = 2.2–28.3º
c = 16.7234 (2) ŵ = 0.33 mm1
α = 79.520 (1)ºT = 100 (2) K
β = 89.031 (1)ºPrism, yellow
γ = 85.258 (1)º0.30 × 0.20 × 0.05 mm
V = 1172.27 (2) Å3
Bruker SMART APEX diffractometer5361 independent reflections
Radiation source: fine-focus sealed tube4771 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.018
T = 100(2) Kθmax = 27.5º
ω scansθmin = 1.2º
Absorption correction: Multi-scan(SADABS; Sheldrick, 1996)h = −9→9
Tmin = 0.908, Tmax = 0.984k = −13→13
11241 measured reflectionsl = −21→21
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.042H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.117  w = 1/[σ2(Fo2) + (0.0573P)2 + 1.0948P] where P = (Fo2 + 2Fc2)/3
S = 1.01(Δ/σ)max = 0.001
5361 reflectionsΔρmax = 0.41 e Å3
360 parametersΔρmin = −0.74 e Å3
47 restraintsExtinction correction: none
Primary atom site location: structure-invariant direct methods
xyzUiso*/UeqOcc. (<1)
Cl10.74259 (7)0.67565 (5)0.56473 (3)0.03176 (13)
Cl20.23984 (7)0.77985 (6)0.56151 (3)0.03809 (15)
O10.54240 (19)0.73990 (13)0.21969 (8)0.0239 (3)
O50.03446 (18)0.95420 (12)0.21807 (8)0.0246 (3)
O20.1961 (3)1.1785 (2)0.17629 (14)0.0204 (4)0.535 (2)
H20.14711.10630.19390.031*0.535 (2)
O2'0.2372 (5)1.0814 (4)0.0932 (2)0.0204 (4)0.328 (3)
H2'0.16881.03970.12920.031*0.328 (3)
O2"0.3318 (13)1.2743 (9)0.0813 (5)0.0204 (4)0.137 (3)
H2"0.40771.31890.10150.031*0.137 (3)
O30.6388 (3)0.98149 (19)0.05581 (12)0.0256 (4)0.650 (3)
H30.74450.94110.04760.038*0.650 (3)
O3'0.8488 (9)1.1295 (10)0.0883 (6)0.0256 (4)0.183 (6)
H3'0.89681.08560.13170.038*0.183 (6)
O3"0.8481 (9)1.0984 (11)0.0690 (7)0.0256 (4)0.166 (6)
H3"0.89951.02270.08940.038*0.166 (6)
O40.6047 (3)1.35087 (18)0.13329 (12)0.0254 (5)0.660 (5)
H40.53751.41320.14920.038*0.660 (5)
O4'0.5213 (6)1.2777 (4)0.2551 (2)0.0254 (5)0.34
H4'0.46311.35310.23940.038*0.340 (5)
O60.3862 (2)0.54296 (15)0.17552 (10)0.0241 (5)0.835 (6)
H60.44030.60310.19250.036*0.835 (6)
O6'0.2819 (11)0.5226 (7)0.0539 (5)0.0241 (5)0.16
H6'0.17800.49130.04620.036*0.165 (6)
O7−0.0249 (2)0.40172 (15)0.12281 (10)0.0251 (5)0.831 (6)
H70.01710.32260.14120.038*0.831 (6)
O7'0.1139 (11)0.3978 (7)0.2403 (4)0.0251 (5)0.17
H7'0.22640.41540.22760.038*0.169 (6)
O8−0.0449 (2)0.81865 (13)0.05073 (8)0.0336 (3)
H8−0.00690.83060.00230.050*
N10.5472 (2)0.99524 (14)0.21010 (9)0.0194 (3)
H1N0.537 (4)0.9209 (17)0.1907 (15)0.043 (7)*
N20.0469 (2)0.70644 (14)0.20403 (9)0.0174 (3)
H2N0.029 (3)0.7936 (11)0.1854 (14)0.033 (6)*
C10.5840 (2)0.72652 (17)0.29646 (11)0.0192 (3)
C20.6121 (3)0.59874 (18)0.34689 (12)0.0271 (4)
H2A0.59900.52090.32430.032*
C30.6579 (3)0.58514 (18)0.42746 (12)0.0268 (4)
H3A0.67600.49830.45980.032*
C40.6782 (2)0.69780 (18)0.46259 (11)0.0232 (4)
C50.6502 (2)0.82333 (18)0.41675 (11)0.0224 (3)
H50.66190.89960.44110.027*
C60.6041 (2)0.84008 (16)0.33387 (11)0.0188 (3)
C70.5840 (2)0.97254 (17)0.28681 (11)0.0216 (3)
H7A0.59841.04630.31310.026*
C80.5387 (2)1.12384 (17)0.15371 (10)0.0203 (3)
C90.3328 (3)1.1578 (2)0.12391 (13)0.0329 (4)
H9A0.33161.23920.08130.039*0.535 (2)
H9B0.29781.08420.09720.039*0.535 (2)
H9C0.25771.18040.17090.039*0.328 (3)
H9D0.33351.24170.08340.039*0.328 (3)
H9E0.29571.09290.09080.039*0.137 (3)
H9F0.24331.15690.17040.039*0.137 (3)
C100.6699 (3)1.1019 (2)0.08285 (13)0.0338 (5)
H10A0.64711.17820.03730.041*0.650 (3)
H10B0.80481.09870.10000.041*0.650 (3)
H10C0.66971.00700.07690.041*0.183 (6)
H10D0.61461.15730.03250.041*0.183 (6)
H10E0.63521.01500.07120.041*0.166 (6)
H10F0.61631.16980.03710.041*0.166 (6)
C110.6064 (3)1.23560 (18)0.19279 (12)0.0289 (4)
H11A0.52041.25140.23820.035*0.660 (5)
H11B0.73721.21060.21460.035*0.660 (5)
H11C0.74081.20830.20920.035*0.340 (5)
H11D0.60951.31500.14890.035*0.340 (5)
C120.0782 (2)0.91510 (17)0.29366 (12)0.0216 (3)
C130.1062 (3)1.00731 (19)0.34634 (14)0.0292 (4)
H130.09161.10060.32530.035*
C140.1531 (3)0.9650 (2)0.42592 (15)0.0335 (5)
H140.17141.02910.45930.040*
C150.1751 (3)0.8282 (2)0.45953 (12)0.0271 (4)
C160.1489 (2)0.73448 (18)0.41255 (11)0.0219 (3)
H160.16190.64190.43570.026*
C170.1027 (2)0.77585 (16)0.32963 (11)0.0187 (3)
C180.0882 (2)0.67582 (16)0.28079 (10)0.0175 (3)
H180.10950.58420.30530.021*
C190.0507 (2)0.61584 (16)0.14497 (10)0.0172 (3)
C200.2570 (2)0.60202 (17)0.11302 (11)0.0213 (3)
H20A0.26210.54650.07010.026*0.835 (6)
H20B0.29590.69170.08840.026*0.835 (6)
H20C0.29630.69240.09020.026*0.165 (6)
H20D0.34250.56360.15930.026*0.165 (6)
C21−0.0160 (2)0.47961 (16)0.18370 (10)0.0197 (3)
H21A0.07470.43440.22670.024*0.831 (6)
H21B−0.14360.49140.20880.024*0.831 (6)
H21C−0.13890.49440.21190.024*0.169 (6)
H21D−0.04070.42990.13980.024*0.169 (6)
C22−0.0847 (3)0.68282 (17)0.07586 (11)0.0229 (3)
H22A−0.06760.63500.02940.027*
H22B−0.21890.67840.09470.027*
U11U22U33U12U13U23
Cl10.0346 (3)0.0301 (2)0.0279 (2)−0.00246 (19)−0.01100 (18)0.00271 (18)
Cl20.0343 (3)0.0474 (3)0.0384 (3)0.0139 (2)−0.0164 (2)−0.0295 (2)
O10.0282 (7)0.0225 (6)0.0243 (6)−0.0092 (5)0.0037 (5)−0.0100 (5)
O50.0241 (6)0.0153 (6)0.0333 (7)−0.0013 (5)0.0054 (5)−0.0018 (5)
O20.0200 (9)0.0169 (9)0.0237 (9)−0.0017 (7)−0.0014 (7)−0.0023 (7)
O2'0.0200 (9)0.0169 (9)0.0237 (9)−0.0017 (7)−0.0014 (7)−0.0023 (7)
O2"0.0200 (9)0.0169 (9)0.0237 (9)−0.0017 (7)−0.0014 (7)−0.0023 (7)
O30.0374 (10)0.0208 (9)0.0184 (9)0.0056 (7)0.0022 (7)−0.0069 (7)
O3'0.0374 (10)0.0208 (9)0.0184 (9)0.0056 (7)0.0022 (7)−0.0069 (7)
O3"0.0374 (10)0.0208 (9)0.0184 (9)0.0056 (7)0.0022 (7)−0.0069 (7)
O40.0304 (10)0.0163 (8)0.0289 (10)0.0014 (7)−0.0012 (7)−0.0035 (7)
O4'0.0304 (10)0.0163 (8)0.0289 (10)0.0014 (7)−0.0012 (7)−0.0035 (7)
O60.0191 (8)0.0217 (8)0.0350 (9)−0.0028 (6)−0.0028 (6)−0.0135 (6)
O6'0.0191 (8)0.0217 (8)0.0350 (9)−0.0028 (6)−0.0028 (6)−0.0135 (6)
O70.0273 (9)0.0185 (8)0.0326 (9)−0.0019 (6)0.0009 (6)−0.0125 (6)
O7'0.0273 (9)0.0185 (8)0.0326 (9)−0.0019 (6)0.0009 (6)−0.0125 (6)
O80.0575 (10)0.0221 (7)0.0194 (6)−0.0016 (6)−0.0017 (6)0.0000 (5)
N10.0198 (7)0.0167 (7)0.0231 (7)−0.0006 (5)−0.0021 (5)−0.0075 (5)
N20.0191 (7)0.0132 (6)0.0200 (7)−0.0008 (5)0.0024 (5)−0.0042 (5)
C10.0150 (7)0.0201 (8)0.0246 (8)−0.0050 (6)0.0038 (6)−0.0082 (6)
C20.0326 (10)0.0189 (8)0.0318 (10)−0.0069 (7)0.0093 (8)−0.0088 (7)
C30.0286 (9)0.0187 (8)0.0315 (10)−0.0017 (7)0.0052 (7)−0.0014 (7)
C40.0185 (8)0.0250 (9)0.0250 (9)−0.0013 (6)−0.0032 (6)−0.0020 (7)
C50.0199 (8)0.0210 (8)0.0275 (9)−0.0013 (6)−0.0078 (7)−0.0068 (7)
C60.0145 (7)0.0181 (8)0.0244 (8)−0.0002 (6)−0.0039 (6)−0.0059 (6)
C70.0211 (8)0.0192 (8)0.0262 (9)0.0016 (6)−0.0069 (6)−0.0094 (7)
C80.0208 (8)0.0198 (8)0.0203 (8)−0.0005 (6)0.0008 (6)−0.0044 (6)
C90.0230 (9)0.0364 (11)0.0336 (10)−0.0047 (8)−0.0029 (8)0.0098 (8)
C100.0383 (11)0.0307 (10)0.0367 (11)−0.0115 (8)0.0183 (9)−0.0150 (8)
C110.0396 (11)0.0174 (8)0.0301 (10)0.0014 (7)−0.0068 (8)−0.0066 (7)
C120.0132 (7)0.0175 (8)0.0360 (10)−0.0019 (6)0.0056 (6)−0.0101 (7)
C130.0212 (9)0.0185 (8)0.0515 (12)−0.0012 (7)−0.0006 (8)−0.0161 (8)
C140.0225 (9)0.0308 (10)0.0549 (13)0.0016 (7)−0.0065 (8)−0.0292 (9)
C150.0175 (8)0.0338 (10)0.0344 (10)0.0042 (7)−0.0049 (7)−0.0202 (8)
C160.0174 (8)0.0230 (8)0.0273 (9)0.0019 (6)−0.0009 (6)−0.0114 (7)
C170.0136 (7)0.0185 (8)0.0261 (8)−0.0013 (6)0.0024 (6)−0.0096 (6)
C180.0161 (7)0.0150 (7)0.0219 (8)−0.0011 (6)0.0022 (6)−0.0052 (6)
C190.0191 (8)0.0158 (7)0.0176 (7)−0.0014 (6)0.0016 (6)−0.0056 (6)
C200.0204 (8)0.0213 (8)0.0236 (8)−0.0034 (6)0.0042 (6)−0.0076 (6)
C210.0211 (8)0.0167 (7)0.0225 (8)−0.0037 (6)0.0018 (6)−0.0054 (6)
C220.0251 (9)0.0214 (8)0.0215 (8)0.0007 (7)−0.0012 (7)−0.0036 (6)
Cl1—C41.7442 (19)C6—C71.431 (2)
Cl2—C151.744 (2)C7—H7A0.9500
O1—C11.302 (2)C8—C111.524 (2)
O5—C121.289 (2)C8—C101.526 (2)
O2—C91.318 (3)C8—C91.528 (3)
O2—H20.8400C9—H9A0.9900
O2'—C91.251 (4)C9—H9B0.9900
O2'—H2'0.8400C9—H9C0.9900
O2"—C91.268 (9)C9—H9D0.9900
O2"—H2"0.8400C9—H9E0.9900
O3—C101.417 (3)C9—H9F0.9900
O3—H30.8400C10—H10A0.9900
O3'—C101.318 (6)C10—H10B0.9900
O3'—H3'0.8400C10—H10C0.9900
O3"—C101.266 (6)C10—H10D0.9900
O3"—H3"0.8400C10—H10E0.9900
O4—C111.394 (3)C10—H10F0.9900
O4—H40.8400C11—H11A0.9900
O4'—C111.313 (4)C11—H11B0.9900
O4'—H4'0.8400C11—H11C0.9900
O6—C201.411 (2)C11—H11D0.9900
O6—H60.8400C12—C131.427 (2)
O6'—C201.389 (6)C12—C171.435 (2)
O6'—H6'0.8400C13—C141.360 (3)
O7—C211.405 (2)C13—H130.9500
O7—H70.8400C14—C151.402 (3)
O7'—C211.428 (6)C14—H140.9500
O7'—H7'0.8400C15—C161.368 (2)
O8—C221.421 (2)C16—C171.409 (2)
O8—H80.8400C16—H160.9500
N1—C71.288 (2)C17—C181.428 (2)
N1—C81.467 (2)C18—H180.9500
N1—H1N0.885 (10)C19—C211.529 (2)
N2—C181.297 (2)C19—C221.532 (2)
N2—C191.468 (2)C19—C201.539 (2)
N2—H2N0.886 (10)C20—H20A0.9900
C1—C21.418 (2)C20—H20B0.9900
C1—C61.430 (2)C20—H20C0.9900
C2—C31.370 (3)C20—H20D0.9900
C2—H2A0.9500C21—H21A0.9900
C3—C41.400 (3)C21—H21B0.9900
C3—H3A0.9500C21—H21C0.9900
C4—C51.368 (2)C21—H21D0.9900
C5—C61.405 (2)C22—H22A0.9900
C5—H50.9500C22—H22B0.9900
C9—O2—H2109.5H10E—C10—H10F105.1
C9—O2'—H2'109.5O4'—C11—O4103.6 (2)
C9—O2"—H2"109.5O4'—C11—C8123.9 (2)
C10—O3—H3109.5O4—C11—C8107.90 (16)
C10—O3'—H3'109.5O4—C11—H11A110.1
C10—O3"—H3"109.5C8—C11—H11A110.1
C11—O4—H4109.5O4'—C11—H11B100.6
C11—O4'—H4'109.5O4—C11—H11B110.1
C20—O6—H6109.5C8—C11—H11B110.1
C20—O6'—H6'109.5H11A—C11—H11B108.4
C21—O7—H7109.5O4'—C11—H11C106.4
C21—O7'—H7'109.5O4—C11—H11C108.0
C22—O8—H8109.5C8—C11—H11C106.4
C7—N1—C8127.86 (14)O4'—C11—H11D106.4
C7—N1—H1N112.8 (18)C8—C11—H11D106.4
C8—N1—H1N119.1 (18)H11B—C11—H11D108.8
C18—N2—C19127.48 (14)H11C—C11—H11D106.4
C18—N2—H2N114.0 (16)O5—C12—C13122.12 (16)
C19—N2—H2N118.0 (16)O5—C12—C17121.79 (15)
O1—C1—C2121.63 (15)C13—C12—C17116.09 (17)
O1—C1—C6121.54 (15)C14—C13—C12121.68 (18)
C2—C1—C6116.83 (16)C14—C13—H13119.2
C3—C2—C1121.40 (16)C12—C13—H13119.2
C3—C2—H2A119.3C13—C14—C15120.98 (17)
C1—C2—H2A119.3C13—C14—H14119.5
C2—C3—C4120.73 (17)C15—C14—H14119.5
C2—C3—H3A119.6C16—C15—C14120.36 (19)
C4—C3—H3A119.6C16—C15—Cl2120.69 (16)
C5—C4—C3120.11 (17)C14—C15—Cl2118.94 (14)
C5—C4—Cl1120.71 (14)C15—C16—C17119.69 (17)
C3—C4—Cl1119.18 (14)C15—C16—H16120.2
C4—C5—C6120.31 (16)C17—C16—H16120.2
C4—C5—H5119.8C16—C17—C18118.51 (15)
C6—C5—H5119.8C16—C17—C12121.20 (15)
C5—C6—C1120.61 (15)C18—C17—C12120.24 (16)
C5—C6—C7118.89 (15)N2—C18—C17121.93 (15)
C1—C6—C7120.46 (15)N2—C18—H18119.0
N1—C7—C6122.31 (15)C17—C18—H18119.0
N1—C7—H7A118.8N2—C19—C21111.20 (13)
C6—C7—H7A118.8N2—C19—C22106.69 (13)
N1—C8—C11112.26 (14)C21—C19—C22109.93 (14)
N1—C8—C10105.88 (15)N2—C19—C20107.43 (13)
C11—C8—C10109.77 (15)C21—C19—C20111.18 (14)
N1—C8—C9108.14 (14)C22—C19—C20110.29 (14)
C11—C8—C9110.66 (16)O6'—C20—O6105.2 (4)
C10—C8—C9110.00 (16)O6'—C20—C19114.2 (3)
O2'—C9—C8124.6 (2)O6—C20—C19111.78 (14)
O2"—C9—C8104.9 (4)O6—C20—H20A109.3
O2—C9—C8119.54 (19)C19—C20—H20A109.3
O2'—C9—H9A103.4O6'—C20—H20B106.9
O2—C9—H9A107.4O6—C20—H20B109.3
C8—C9—H9A107.4C19—C20—H20B109.3
O2"—C9—H9B118.1H20A—C20—H20B107.9
O2—C9—H9B107.4O6'—C20—H20C108.7
C8—C9—H9B107.4O6—C20—H20C108.0
H9A—C9—H9B107.0C19—C20—H20C108.7
O2'—C9—H9C106.2H20A—C20—H20C109.8
C8—C9—H9C106.2O6'—C20—H20D108.7
H9A—C9—H9C108.2C19—C20—H20D108.7
H9B—C9—H9C120.1H20A—C20—H20D112.6
O2'—C9—H9D106.2H20B—C20—H20D109.0
O2—C9—H9D106.2H20C—C20—H20D107.6
C8—C9—H9D106.2O7—C21—O7'101.9 (3)
H9B—C9—H9D109.8O7—C21—C19108.48 (14)
O2"—C9—H9E110.8O7'—C21—C19115.5 (3)
O2—C9—H9E110.1O7—C21—H21A110.0
C8—C9—H9E110.8C19—C21—H21A110.0
O2"—C9—H9F110.8O7—C21—H21B110.0
C8—C9—H9F110.8O7'—C21—H21B110.7
H9E—C9—H9F108.8C19—C21—H21B110.0
O3'—C10—C8116.5 (5)H21A—C21—H21B108.4
O3—C10—C8111.74 (16)O7—C21—H21C114.3
O3—C10—H10A109.3O7'—C21—H21C108.4
C8—C10—H10A109.3C19—C21—H21C108.4
O3—C10—H10B109.3H21A—C21—H21C105.6
C8—C10—H10B109.3O7'—C21—H21D108.4
H10A—C10—H10B107.9C19—C21—H21D108.4
O3'—C10—H10C108.2H21A—C21—H21D116.7
C8—C10—H10C108.2H21B—C21—H21D103.1
O3'—C10—H10D108.2H21C—C21—H21D107.5
C8—C10—H10D108.2O8—C22—C19109.62 (14)
H10C—C10—H10D107.3O8—C22—H22A109.7
C8—C10—H10E103.1C19—C22—H22A109.7
O3"—C10—H10F103.1O8—C22—H22B109.7
O3'—C10—H10F104.6C19—C22—H22B109.7
O3—C10—H10F101.4H22A—C22—H22B108.2
C8—C10—H10F103.1
O1—C1—C2—C3179.32 (17)C9—C8—C11—O4'58.1 (3)
C6—C1—C2—C3−0.5 (3)N1—C8—C11—O4176.23 (16)
C1—C2—C3—C40.0 (3)C10—C8—C11—O458.8 (2)
C2—C3—C4—C50.8 (3)C9—C8—C11—O4−62.8 (2)
C2—C3—C4—Cl1−178.35 (15)O5—C12—C13—C14−179.70 (17)
C3—C4—C5—C6−1.1 (3)C17—C12—C13—C140.0 (3)
Cl1—C4—C5—C6178.02 (13)C12—C13—C14—C15−0.3 (3)
C4—C5—C6—C10.6 (3)C13—C14—C15—C16−0.2 (3)
C4—C5—C6—C7−177.26 (16)C13—C14—C15—Cl2178.80 (15)
O1—C1—C6—C5−179.64 (15)C14—C15—C16—C171.0 (3)
C2—C1—C6—C50.2 (2)Cl2—C15—C16—C17−177.95 (13)
O1—C1—C6—C7−1.8 (2)C15—C16—C17—C18176.05 (16)
C2—C1—C6—C7178.03 (16)C15—C16—C17—C12−1.4 (3)
C8—N1—C7—C6−174.53 (16)O5—C12—C17—C16−179.45 (15)
C5—C6—C7—N1178.05 (16)C13—C12—C17—C160.9 (2)
C1—C6—C7—N10.2 (3)O5—C12—C17—C183.2 (2)
C7—N1—C8—C117.8 (2)C13—C12—C17—C18−176.51 (15)
C7—N1—C8—C10127.59 (19)C19—N2—C18—C17171.78 (15)
C7—N1—C8—C9−114.5 (2)C16—C17—C18—N2−179.76 (15)
N1—C8—C9—O2'−52.8 (3)C12—C17—C18—N2−2.3 (2)
C11—C8—C9—O2'−176.2 (3)C18—N2—C19—C2136.7 (2)
C10—C8—C9—O2'62.4 (3)C18—N2—C19—C22156.57 (16)
N1—C8—C9—O2"174.6 (5)C18—N2—C19—C20−85.16 (19)
C11—C8—C9—O2"51.2 (5)N2—C19—C20—O6'−177.7 (4)
C10—C8—C9—O2"−70.2 (5)C21—C19—C20—O6'60.4 (4)
N1—C8—C9—O263.7 (2)C22—C19—C20—O6'−61.8 (4)
C11—C8—C9—O2−59.6 (2)N2—C19—C20—O662.94 (17)
C10—C8—C9—O2178.90 (19)C21—C19—C20—O6−58.93 (18)
N1—C8—C10—O3"−80.6 (7)C22—C19—C20—O6178.86 (14)
C11—C8—C10—O3"40.8 (7)N2—C19—C21—O7175.00 (14)
C9—C8—C10—O3"162.8 (7)C22—C19—C21—O757.08 (18)
N1—C8—C10—O3'−92.1 (5)C20—C19—C21—O7−65.33 (18)
C11—C8—C10—O3'29.3 (5)N2—C19—C21—O7'−71.5 (4)
C9—C8—C10—O3'151.3 (4)C22—C19—C21—O7'170.6 (4)
N1—C8—C10—O346.0 (2)C20—C19—C21—O7'48.2 (4)
C11—C8—C10—O3167.35 (18)N2—C19—C22—O848.05 (18)
C9—C8—C10—O3−70.7 (2)C21—C19—C22—O8168.73 (14)
N1—C8—C11—O4'−62.9 (3)C20—C19—C22—O8−68.33 (18)
C10—C8—C11—O4'179.7 (3)
D—H···AD—HH···AD···AD—H···A
N1—H1n···O10.87 (1)1.82 (2)2.582 (2)143 (2)
N2—H2n···O50.87 (1)1.82 (2)2.573 (2)141 (2)
  3 in total

1.  2-[[tris(hydroxymethyl)methyl]aminomethylene]cyclohexa-3,5-dien-1(2H)-one and its 6-hydroxy and 6-methoxy derivatives.

Authors:  Mustafa Odabaşoğlu; Cigdem Albayrak; Orhan Büyükgüngör; Peter Lönnecke
Journal:  Acta Crystallogr C       Date:  2003-10-11       Impact factor: 1.172

2.  Alkoxo Bound Monooxo- and Dioxovanadium(V) Complexes: Synthesis, Characterization, X-ray Crystal Structures, and Solution Reactivity Studies.

Authors:  Gebray Asgedom; Alavattam Sreedhara; Jussi Kivikoski; Jussi Valkonen; Erkki Kolehmainen; Chebrolu P. Rao
Journal:  Inorg Chem       Date:  1996-09-11       Impact factor: 5.165

3.  A short history of SHELX.

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

  3 in total
  4 in total

1.  (2-{[1,1-Bis(hydroxy-meth-yl)-2-oxidoeth-yl]imino-meth-yl}-4-chloro-phenolato-κN,O,O')dibutyl-tin(IV).

Authors:  Reza Reisi; Misni Misran; Kong Mun Lo; Seik Weng Ng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-03-31

2.  (E)-2-[(2-Hydroxy-ethyl)iminiometh-yl]-6-methoxy-phenolate.

Authors:  Guo-Xia Tan; Xi-Cheng Liu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-02-21

3.  (2-{[1,1-Bis(hy-droxy-meth-yl)-2-oxidoeth-yl]imino-meth-yl}-4-chloro-phenolato-κO,N,O')dibutyl-tin(IV).

Authors:  See Mun Lee; Hapipah Mohd Ali; Kong Mun Lo
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-06-16

4.  (E)-4-Hy-droxy-2-{[(2-phenyl-eth-yl)iminium-yl]meth-yl}phenolate.

Authors:  David Ortegon-Reyna; Cesar Garcias-Morales; Efren V García-Báez; Armando Ariza-Castolo; Francisco J Martínez-Martínez
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-06-13
  4 in total

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