Literature DB >> 21837122

2-[(E)-2-(Benzyl-idene-amino)-eth-yl]-3',6'-bis-(diethyl-amino)-spiro-[isoindoline-1,9'-xanthen]-3-one.

Zhen Wei1, Xujun Zheng, Junjun Bai, Xiaohong Zhai, Lili Song.   

Abstract

In the title compound, C(37)H(40)N(4)O(2), the xanthene and spiro-lactam rings are almost planar, with r.m.s. deviations from the mean planes of 0.223 (2) and 0.057 (2) Å, respectively, and form a dihedral angle of 85.76 (3)°. The dihedral angle between the xanthene mean plane and the benzene ring is 87.16 (5)°. One of the two ethyl groups of one of the diethyl-amino groups is disordered over two sets of sites [0.76 (1):0.24 (1)].

Entities:  

Year:  2011        PMID: 21837122      PMCID: PMC3151774          DOI: 10.1107/S1600536811020320

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


Related literature

For related structures and background to rhodamine dyes, see: Xu et al. (2010a ▶,b ▶); Zhang et al. (2008 ▶); Tian et al. (2008 ▶); Kwon et al. (2005 ▶); Wu et al. (2007 ▶).

Experimental

Crystal data

C37H40N4O2 M = 572.73 Triclinic, a = 9.842 (2) Å b = 13.151 (3) Å c = 13.552 (3) Å α = 74.43 (3)° β = 81.92 (3)° γ = 69.12 (3)° V = 1576.7 (7) Å3 Z = 2 Mo Kα radiation μ = 0.08 mm−1 T = 293 K 0.26 × 0.22 × 0.20 mm

Data collection

Rigaku Saturn diffractometer Absorption correction: multi-scan (CrystalClear; Rigaku, 2008 ▶) T min = 0.981, T max = 0.985 17336 measured reflections 6168 independent reflections 4273 reflections with I > 2σ(I) R int = 0.033

Refinement

R[F 2 > 2σ(F 2)] = 0.057 wR(F 2) = 0.174 S = 1.06 6168 reflections 399 parameters 2 restraints H-atom parameters constrained Δρmax = 0.29 e Å−3 Δρmin = −0.24 e Å−3 Data collection: CrystalClear (Rigaku, 2008 ▶); cell refinement: CrystalClear; data reduction: CrystalClear; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: SHELXTL (Sheldrick, 2008 ▶); software used to prepare material for publication: SHELXL97. Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S1600536811020320/bg2398sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536811020320/bg2398Isup2.hkl Supplementary material file. DOI: 10.1107/S1600536811020320/bg2398Isup3.cdx Supplementary material file. DOI: 10.1107/S1600536811020320/bg2398Isup4.cml Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C37H40N4O2Z = 2
Mr = 572.73F(000) = 612
Triclinic, P1Dx = 1.206 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 9.842 (2) ÅCell parameters from 3876 reflections
b = 13.151 (3) Åθ = 1.6–29.0°
c = 13.552 (3) ŵ = 0.08 mm1
α = 74.43 (3)°T = 293 K
β = 81.92 (3)°Prism, colourless
γ = 69.12 (3)°0.26 × 0.22 × 0.20 mm
V = 1576.7 (7) Å3
Rigaku Saturn diffractometer6168 independent reflections
Radiation source: fine-focus sealed tube4273 reflections with I > 2σ(I)
graphiteRint = 0.033
Detector resolution: 7.31 pixels mm-1θmax = 26.0°, θmin = 1.6°
ω scansh = −12→12
Absorption correction: multi-scan (CrystalClear; Rigaku, 2008)k = −16→16
Tmin = 0.981, Tmax = 0.985l = −16→16
17336 measured reflections
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.057Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.174H-atom parameters constrained
S = 1.06w = 1/[σ2(Fo2) + (0.1016P)2] where P = (Fo2 + 2Fc2)/3
6168 reflections(Δ/σ)max < 0.001
399 parametersΔρmax = 0.29 e Å3
2 restraintsΔρmin = −0.24 e Å3
Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR andgoodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.
xyzUiso*/UeqOcc. (<1)
O10.33256 (15)0.41003 (11)0.03815 (10)0.0723 (4)
O20.36695 (14)0.00487 (9)0.43694 (9)0.0579 (4)
N10.31962 (15)0.25956 (11)0.16827 (10)0.0456 (4)
N2−0.00271 (18)0.22023 (14)0.08727 (13)0.0650 (5)
N3−0.04621 (17)0.22186 (14)0.60535 (13)0.0665 (5)
N40.72011 (19)−0.26509 (12)0.27732 (12)0.0652 (5)
C10.37105 (19)0.34525 (14)0.12145 (13)0.0506 (4)
C20.47929 (18)0.34194 (13)0.18879 (13)0.0487 (4)
C30.5722 (2)0.40412 (15)0.17296 (16)0.0628 (5)
H30.56700.46260.11530.075*
C40.6718 (2)0.37619 (17)0.24543 (18)0.0741 (6)
H40.73550.41630.23630.089*
C50.6800 (2)0.28913 (18)0.33248 (17)0.0697 (6)
H50.74860.27190.38040.084*
C60.5866 (2)0.22835 (16)0.34780 (13)0.0569 (5)
H60.59040.17080.40610.068*
C70.48760 (18)0.25501 (13)0.27459 (12)0.0451 (4)
C80.38313 (18)0.19473 (13)0.26923 (11)0.0423 (4)
C90.26660 (18)0.20220 (13)0.35566 (11)0.0418 (4)
C100.26648 (18)0.10992 (13)0.43410 (12)0.0451 (4)
C110.16418 (19)0.11548 (15)0.51642 (13)0.0529 (4)
H110.16960.05120.56790.063*
C120.05450 (19)0.21522 (15)0.52287 (13)0.0515 (4)
C130.0518 (2)0.30963 (15)0.44214 (13)0.0551 (5)
H13−0.02140.37790.44240.066*
C140.1558 (2)0.30175 (14)0.36355 (13)0.0526 (4)
H140.15230.36610.31280.063*
C150.46646 (17)0.07377 (13)0.26878 (11)0.0423 (4)
C160.45792 (18)−0.01265 (13)0.35126 (12)0.0446 (4)
C170.54006 (19)−0.12331 (14)0.35451 (13)0.0512 (4)
H170.5299−0.17860.41160.061*
C180.63747 (19)−0.15355 (14)0.27427 (13)0.0500 (4)
C190.6473 (2)−0.06638 (15)0.18986 (13)0.0585 (5)
H190.7104−0.08290.13410.070*
C200.5653 (2)0.04237 (15)0.18886 (13)0.0553 (5)
H200.57580.09810.13230.066*
C210.2309 (2)0.22241 (15)0.11800 (14)0.0547 (5)
H21A0.25800.14160.14120.066*
H21B0.25390.23970.04470.066*
C220.0696 (2)0.27255 (18)0.13600 (17)0.0683 (6)
H22A0.04430.25970.20900.082*
H22B0.03830.35270.10700.082*
C23−0.1125 (2)0.28245 (17)0.03626 (15)0.0606 (5)
H23−0.14290.35930.03030.073*
C24−0.1941 (2)0.23795 (17)−0.01401 (14)0.0579 (5)
C25−0.1574 (2)0.12469 (18)−0.00607 (15)0.0657 (5)
H25−0.07940.07490.03280.079*
C26−0.2341 (3)0.0835 (2)−0.05482 (16)0.0771 (6)
H26−0.20640.0070−0.05010.093*
C27−0.3511 (3)0.1566 (3)−0.10997 (18)0.0909 (8)
H27−0.40450.1298−0.14200.109*
C28−0.3891 (3)0.2687 (3)−0.1178 (2)0.1100 (10)
H28−0.46880.3180−0.15520.132*
C29−0.3110 (3)0.3104 (2)−0.07097 (19)0.0887 (7)
H29−0.33730.3872−0.07800.106*
C30−0.1847 (2)0.31369 (18)0.59963 (17)0.0753 (6)
H30A−0.26000.28400.63560.090*
H30B−0.20900.34410.52830.090*
C31−0.1861 (3)0.4074 (2)0.6441 (2)0.1015 (8)
H31A−0.27970.46510.63600.152*
H31B−0.11220.43780.60890.152*
H31C−0.16710.37910.71570.152*
C32−0.0309 (2)0.12577 (18)0.69285 (16)0.0714 (6)
H32A−0.07780.15260.75330.086*
H32B0.07180.08780.70520.086*
C33−0.0946 (3)0.0433 (2)0.6787 (2)0.1069 (9)
H33A−0.0736−0.02040.73620.160*
H33B−0.05290.01940.61690.160*
H33C−0.19810.07780.67400.160*
C340.8377 (3)−0.2893 (2)0.1969 (2)0.0724 (8)0.76
H34A0.9211−0.27070.20640.087*0.76
H34B0.8012−0.24560.12940.087*0.76
C350.8722 (4)−0.4042 (3)0.1772 (3)0.0838 (11)0.76
H35A0.8985−0.46030.23990.101*0.76
H35B0.9519−0.41700.12710.101*0.76
H35C0.7883−0.40830.15210.101*0.76
C34'0.7532 (10)−0.3164 (7)0.1892 (6)0.0724 (8)0.24
H34C0.7230−0.25660.12840.087*0.24
H34D0.6966−0.36550.19670.087*0.24
C35'0.9113 (12)−0.3765 (11)0.1716 (13)0.0838 (11)0.24
H35D0.9623−0.32350.15120.101*0.24
H35E0.9241−0.41540.11850.101*0.24
H35F0.9493−0.42940.23380.101*0.24
C360.7264 (2)−0.34727 (17)0.37557 (17)0.0726 (6)
H36A0.7233−0.31190.43050.087*
H36B0.8185−0.40800.37720.087*
C370.6059 (3)−0.3945 (2)0.3947 (2)0.0971 (8)
H37A0.5141−0.33460.38950.146*
H37B0.6116−0.44300.46220.146*
H37C0.6141−0.43640.34470.146*
U11U22U33U12U13U23
O10.0802 (10)0.0692 (9)0.0529 (8)−0.0277 (8)−0.0096 (7)0.0163 (7)
O20.0672 (8)0.0433 (7)0.0453 (7)−0.0118 (6)0.0151 (6)0.0002 (5)
N10.0533 (8)0.0474 (8)0.0364 (7)−0.0224 (7)−0.0069 (6)−0.0005 (6)
N20.0600 (10)0.0694 (10)0.0723 (11)−0.0221 (8)−0.0126 (9)−0.0222 (8)
N30.0568 (10)0.0709 (10)0.0628 (10)−0.0188 (8)0.0170 (8)−0.0147 (8)
N40.0704 (11)0.0488 (9)0.0634 (10)−0.0074 (8)0.0043 (8)−0.0128 (7)
C10.0550 (10)0.0468 (9)0.0428 (9)−0.0187 (8)0.0009 (8)0.0016 (7)
C20.0527 (10)0.0439 (9)0.0494 (10)−0.0218 (8)0.0033 (8)−0.0060 (7)
C30.0675 (12)0.0515 (11)0.0722 (13)−0.0327 (10)0.0081 (10)−0.0077 (9)
C40.0715 (14)0.0742 (14)0.0979 (17)−0.0446 (12)0.0074 (12)−0.0334 (13)
C50.0708 (13)0.0849 (15)0.0701 (13)−0.0379 (12)−0.0069 (10)−0.0277 (11)
C60.0650 (12)0.0646 (11)0.0467 (10)−0.0285 (10)−0.0059 (9)−0.0114 (8)
C70.0509 (9)0.0464 (9)0.0412 (9)−0.0225 (8)0.0015 (7)−0.0091 (7)
C80.0510 (9)0.0420 (9)0.0347 (8)−0.0213 (7)−0.0037 (7)−0.0017 (6)
C90.0488 (9)0.0409 (9)0.0370 (8)−0.0185 (8)−0.0020 (7)−0.0066 (7)
C100.0479 (9)0.0425 (9)0.0430 (9)−0.0172 (8)0.0007 (7)−0.0059 (7)
C110.0591 (11)0.0514 (10)0.0461 (10)−0.0249 (9)0.0088 (8)−0.0054 (8)
C120.0502 (10)0.0578 (11)0.0507 (10)−0.0227 (9)0.0050 (8)−0.0171 (8)
C130.0559 (11)0.0497 (10)0.0541 (10)−0.0115 (8)−0.0003 (8)−0.0126 (8)
C140.0643 (11)0.0449 (10)0.0444 (9)−0.0184 (9)−0.0008 (8)−0.0044 (7)
C150.0466 (9)0.0437 (9)0.0367 (8)−0.0194 (7)−0.0008 (7)−0.0042 (7)
C160.0475 (9)0.0474 (10)0.0396 (8)−0.0205 (8)0.0034 (7)−0.0077 (7)
C170.0565 (10)0.0426 (10)0.0482 (10)−0.0155 (8)0.0019 (8)−0.0041 (7)
C180.0472 (9)0.0503 (10)0.0510 (10)−0.0134 (8)−0.0032 (8)−0.0131 (8)
C190.0634 (12)0.0615 (12)0.0445 (10)−0.0178 (10)0.0106 (8)−0.0137 (8)
C200.0623 (11)0.0529 (11)0.0434 (9)−0.0189 (9)0.0073 (8)−0.0051 (8)
C210.0599 (11)0.0590 (11)0.0493 (10)−0.0219 (9)−0.0108 (8)−0.0125 (8)
C220.0575 (12)0.0759 (13)0.0827 (14)−0.0222 (10)−0.0096 (10)−0.0340 (11)
C230.0518 (11)0.0662 (12)0.0636 (12)−0.0170 (10)−0.0020 (9)−0.0192 (10)
C240.0488 (10)0.0715 (13)0.0538 (11)−0.0186 (9)−0.0001 (8)−0.0188 (9)
C250.0618 (12)0.0814 (15)0.0604 (12)−0.0309 (11)−0.0017 (9)−0.0183 (10)
C260.0852 (16)0.1079 (17)0.0617 (13)−0.0579 (14)0.0115 (12)−0.0309 (12)
C270.0702 (15)0.161 (3)0.0698 (15)−0.0571 (17)0.0031 (12)−0.0519 (16)
C280.0725 (17)0.159 (3)0.098 (2)−0.0152 (18)−0.0340 (15)−0.047 (2)
C290.0691 (14)0.1021 (18)0.0879 (17)−0.0075 (13)−0.0237 (13)−0.0300 (14)
C300.0560 (12)0.0891 (15)0.0778 (14)−0.0188 (11)0.0111 (10)−0.0295 (12)
C310.103 (2)0.0996 (19)0.0962 (18)−0.0119 (15)−0.0012 (15)−0.0454 (15)
C320.0767 (14)0.0844 (14)0.0616 (12)−0.0423 (12)0.0242 (10)−0.0242 (10)
C330.115 (2)0.114 (2)0.116 (2)−0.0718 (18)0.0348 (17)−0.0437 (17)
C340.0742 (19)0.0536 (15)0.0874 (18)−0.0204 (13)0.0190 (16)−0.0261 (13)
C350.098 (3)0.072 (2)0.0880 (19)−0.0393 (16)0.0252 (19)−0.0309 (19)
C34'0.0742 (19)0.0536 (15)0.0874 (18)−0.0204 (13)0.0190 (16)−0.0261 (13)
C35'0.098 (3)0.072 (2)0.0880 (19)−0.0393 (16)0.0252 (19)−0.0309 (19)
C360.0678 (13)0.0586 (12)0.0777 (14)−0.0027 (11)−0.0078 (11)−0.0169 (11)
C370.122 (2)0.0702 (15)0.0990 (19)−0.0350 (15)−0.0047 (17)−0.0172 (13)
O1—C11.2319 (19)C21—H21A0.9700
O2—C101.377 (2)C21—H21B0.9700
O2—C161.3810 (19)C22—H22A0.9700
N1—C11.364 (2)C22—H22B0.9700
N1—C211.455 (2)C23—C241.468 (3)
N1—C81.491 (2)C23—H230.9300
N2—C231.261 (2)C24—C291.378 (3)
N2—C221.463 (2)C24—C251.379 (3)
N3—C121.385 (2)C25—C261.387 (3)
N3—C301.459 (3)C25—H250.9300
N3—C321.461 (3)C26—C271.370 (3)
N4—C181.393 (2)C26—H260.9300
N4—C361.466 (3)C27—C281.364 (4)
N4—C341.482 (3)C27—H270.9300
N4—C34'1.467 (7)C28—C291.386 (3)
C1—C21.479 (2)C28—H280.9300
C2—C71.383 (2)C29—H290.9300
C2—C31.391 (2)C30—C311.506 (3)
C3—C41.371 (3)C30—H30A0.9700
C3—H30.9300C30—H30B0.9700
C4—C51.395 (3)C31—H31A0.9600
C4—H40.9300C31—H31B0.9600
C5—C61.381 (3)C31—H31C0.9600
C5—H50.9300C32—C331.496 (3)
C6—C71.378 (2)C32—H32A0.9700
C6—H60.9300C32—H32B0.9700
C7—C81.524 (2)C33—H33A0.9600
C8—C151.509 (2)C33—H33B0.9600
C8—C91.517 (2)C33—H33C0.9600
C9—C101.382 (2)C34—C351.515 (4)
C9—C141.393 (2)C34—H34A0.9700
C10—C111.393 (2)C34—H34B0.9801
C11—C121.385 (3)C35—H35A0.9600
C11—H110.9300C35—H35B0.9600
C12—C131.412 (2)C35—H35C0.9600
C13—C141.367 (2)C34'—C35'1.492 (9)
C13—H130.9300C34'—H34C0.9696
C14—H140.9300C34'—H34D0.9710
C15—C161.381 (2)C35'—H35D0.9600
C15—C201.395 (2)C35'—H35E0.9600
C16—C171.382 (2)C35'—H35F0.9600
C17—C181.388 (2)C36—C371.488 (3)
C17—H170.9300C36—H36A0.9700
C18—C191.406 (2)C36—H36B0.9700
C19—C201.366 (2)C37—H37A0.9600
C19—H190.9300C37—H37B0.9600
C20—H200.9300C37—H37C0.9600
C21—C221.498 (3)
C10—O2—C16118.54 (12)N2—C22—C21108.56 (16)
C1—N1—C21123.41 (14)N2—C22—H22A110.0
C1—N1—C8113.61 (13)C21—C22—H22A110.0
C21—N1—C8122.21 (13)N2—C22—H22B110.0
C23—N2—C22118.20 (18)C21—C22—H22B110.0
C12—N3—C30121.57 (16)H22A—C22—H22B108.4
C12—N3—C32120.37 (16)N2—C23—C24122.38 (19)
C30—N3—C32116.85 (16)N2—C23—H23118.8
C18—N4—C36118.08 (16)C24—C23—H23118.8
C18—N4—C34118.14 (17)C29—C24—C25118.5 (2)
C36—N4—C34119.76 (17)C29—C24—C23119.7 (2)
C18—N4—C34'124.8 (4)C25—C24—C23121.83 (18)
C36—N4—C34'112.6 (4)C24—C25—C26121.4 (2)
O1—C1—N1124.55 (17)C24—C25—H25119.3
O1—C1—C2128.61 (16)C26—C25—H25119.3
N1—C1—C2106.83 (13)C27—C26—C25119.3 (2)
C7—C2—C3120.98 (17)C27—C26—H26120.3
C7—C2—C1108.63 (14)C25—C26—H26120.3
C3—C2—C1130.17 (16)C28—C27—C26119.8 (2)
C4—C3—C2117.64 (17)C28—C27—H27120.1
C4—C3—H3121.2C26—C27—H27120.1
C2—C3—H3121.2C27—C28—C29121.0 (2)
C3—C4—C5121.62 (18)C27—C28—H28119.5
C3—C4—H4119.2C29—C28—H28119.5
C5—C4—H4119.2C24—C29—C28119.9 (3)
C6—C5—C4120.29 (19)C24—C29—H29120.0
C6—C5—H5119.9C28—C29—H29120.0
C4—C5—H5119.9N3—C30—C31114.5 (2)
C7—C6—C5118.37 (17)N3—C30—H30A108.6
C7—C6—H6120.8C31—C30—H30A108.6
C5—C6—H6120.8N3—C30—H30B108.6
C6—C7—C2121.08 (16)C31—C30—H30B108.6
C6—C7—C8128.26 (14)H30A—C30—H30B107.6
C2—C7—C8110.54 (14)C30—C31—H31A109.5
N1—C8—C15111.68 (13)C30—C31—H31B109.5
N1—C8—C9111.33 (13)H31A—C31—H31B109.5
C15—C8—C9110.18 (12)C30—C31—H31C109.5
N1—C8—C7100.36 (12)H31A—C31—H31C109.5
C15—C8—C7110.20 (13)H31B—C31—H31C109.5
C9—C8—C7112.79 (13)N3—C32—C33113.9 (2)
C10—C9—C14115.44 (15)N3—C32—H32A108.8
C10—C9—C8121.58 (14)C33—C32—H32A108.8
C14—C9—C8122.95 (13)N3—C32—H32B108.8
O2—C10—C9122.77 (15)C33—C32—H32B108.8
O2—C10—C11114.51 (14)H32A—C32—H32B107.7
C9—C10—C11122.72 (16)C32—C33—H33A109.5
C12—C11—C10121.02 (16)C32—C33—H33B109.5
C12—C11—H11119.5H33A—C33—H33B109.5
C10—C11—H11119.5C32—C33—H33C109.5
N3—C12—C11121.37 (16)H33A—C33—H33C109.5
N3—C12—C13121.87 (16)H33B—C33—H33C109.5
C11—C12—C13116.76 (16)N4—C34—C35112.9 (2)
C14—C13—C12120.69 (16)N4—C34—H34A112.6
C14—C13—H13119.7C35—C34—H34A115.5
C12—C13—H13119.7N4—C34—H34B109.8
C13—C14—C9123.34 (15)C35—C34—H34B97.1
C13—C14—H14118.3H34A—C34—H34B107.5
C9—C14—H14118.3N4—C34'—C35'113.8 (9)
C16—C15—C20115.59 (15)N4—C34'—H34C107.5
C16—C15—C8121.89 (14)C35'—C34'—H34C106.6
C20—C15—C8122.34 (14)N4—C34'—H34D109.6
O2—C16—C15122.60 (15)C35'—C34'—H34D111.1
O2—C16—C17114.83 (14)H34B—C34'—H34D146.2
C15—C16—C17122.57 (16)H34C—C34'—H34D107.9
C16—C17—C18121.29 (15)C34'—C35'—H35D109.5
C16—C17—H17119.4C34'—C35'—H35E109.5
C18—C17—H17119.4H35D—C35'—H35E109.5
C17—C18—N4121.37 (16)C34'—C35'—H35F109.5
C17—C18—C19116.72 (16)H35D—C35'—H35F109.5
N4—C18—C19121.91 (16)H35E—C35'—H35F109.5
C20—C19—C18120.76 (16)N4—C36—C37113.50 (19)
C20—C19—H19119.6N4—C36—H36A108.9
C18—C19—H19119.6C37—C36—H36A108.9
C19—C20—C15123.05 (16)N4—C36—H36B108.9
C19—C20—H20118.5C37—C36—H36B108.9
C15—C20—H20118.5H36A—C36—H36B107.7
N1—C21—C22115.50 (15)C36—C37—H37A109.5
N1—C21—H21A108.4C36—C37—H37B109.5
C22—C21—H21A108.4H37A—C37—H37B109.5
N1—C21—H21B108.4C36—C37—H37C109.5
C22—C21—H21B108.4H37A—C37—H37C109.5
H21A—C21—H21B107.5H37B—C37—H37C109.5
C21—N1—C1—O110.6 (3)N1—C8—C15—C16−138.91 (15)
C8—N1—C1—O1−179.33 (17)C9—C8—C15—C16−14.6 (2)
C21—N1—C1—C2−168.62 (15)C7—C8—C15—C16110.44 (17)
C8—N1—C1—C21.50 (19)N1—C8—C15—C2046.1 (2)
O1—C1—C2—C7−179.92 (18)C9—C8—C15—C20170.38 (15)
N1—C1—C2—C7−0.79 (19)C7—C8—C15—C20−64.54 (19)
O1—C1—C2—C3−5.3 (3)C10—O2—C16—C159.4 (2)
N1—C1—C2—C3173.79 (18)C10—O2—C16—C17−170.81 (14)
C7—C2—C3—C4−0.1 (3)C20—C15—C16—O2179.04 (15)
C1—C2—C3—C4−174.11 (18)C8—C15—C16—O23.7 (2)
C2—C3—C4—C5−0.4 (3)C20—C15—C16—C17−0.8 (2)
C3—C4—C5—C60.0 (3)C8—C15—C16—C17−176.08 (15)
C4—C5—C6—C70.9 (3)O2—C16—C17—C18−179.34 (15)
C5—C6—C7—C2−1.4 (3)C15—C16—C17—C180.5 (3)
C5—C6—C7—C8174.27 (18)C16—C17—C18—N4−179.84 (16)
C3—C2—C7—C61.0 (3)C16—C17—C18—C19−0.4 (3)
C1—C2—C7—C6176.16 (16)C36—N4—C18—C17−13.2 (3)
C3—C2—C7—C8−175.35 (16)C34—N4—C18—C17−170.6 (2)
C1—C2—C7—C8−0.18 (19)C34'—N4—C18—C17141.0 (5)
C1—N1—C8—C15−118.30 (15)C36—N4—C18—C19167.39 (18)
C21—N1—C8—C1552.0 (2)C34—N4—C18—C1910.0 (3)
C1—N1—C8—C9118.08 (15)C34'—N4—C18—C19−38.4 (5)
C21—N1—C8—C9−71.67 (19)C17—C18—C19—C200.7 (3)
C1—N1—C8—C7−1.53 (17)N4—C18—C19—C20−179.88 (18)
C21—N1—C8—C7168.72 (15)C18—C19—C20—C15−1.1 (3)
C6—C7—C8—N1−175.03 (17)C16—C15—C20—C191.1 (3)
C2—C7—C8—N10.97 (17)C8—C15—C20—C19176.36 (16)
C6—C7—C8—C15−57.2 (2)C1—N1—C21—C22−94.8 (2)
C2—C7—C8—C15118.84 (15)C8—N1—C21—C2295.9 (2)
C6—C7—C8—C966.4 (2)C23—N2—C22—C21−135.87 (19)
C2—C7—C8—C9−117.58 (15)N1—C21—C22—N2−175.59 (14)
N1—C8—C9—C10138.75 (15)C22—N2—C23—C24−178.91 (17)
C15—C8—C9—C1014.3 (2)N2—C23—C24—C29−178.3 (2)
C7—C8—C9—C10−109.32 (17)N2—C23—C24—C251.7 (3)
N1—C8—C9—C14−43.2 (2)C29—C24—C25—C260.7 (3)
C15—C8—C9—C14−167.67 (14)C23—C24—C25—C26−179.25 (17)
C7—C8—C9—C1468.73 (19)C24—C25—C26—C27−1.6 (3)
C16—O2—C10—C9−9.7 (2)C25—C26—C27—C281.1 (4)
C16—O2—C10—C11169.93 (14)C26—C27—C28—C290.2 (4)
C14—C9—C10—O2178.82 (15)C25—C24—C29—C280.6 (3)
C8—C9—C10—O2−3.0 (2)C23—C24—C29—C28−179.4 (2)
C14—C9—C10—C11−0.8 (2)C27—C28—C29—C24−1.0 (4)
C8—C9—C10—C11177.40 (15)C12—N3—C30—C31−97.3 (2)
O2—C10—C11—C12−178.66 (15)C32—N3—C30—C3195.2 (2)
C9—C10—C11—C121.0 (3)C12—N3—C32—C33−84.8 (2)
C30—N3—C12—C11−161.22 (18)C30—N3—C32—C3382.9 (2)
C32—N3—C12—C115.9 (3)C18—N4—C34—C35−153.8 (3)
C30—N3—C12—C1319.7 (3)C36—N4—C34—C3549.1 (4)
C32—N3—C12—C13−173.26 (17)C34'—N4—C34—C35−42.0 (6)
C10—C11—C12—N3−178.91 (17)C18—N4—C34'—C35'128.0 (7)
C10—C11—C12—C130.3 (3)C36—N4—C34'—C35'−76.5 (9)
N3—C12—C13—C14177.52 (17)C34—N4—C34'—C35'33.5 (7)
C11—C12—C13—C14−1.6 (3)C18—N4—C36—C3787.3 (2)
C12—C13—C14—C91.9 (3)C34—N4—C36—C37−115.6 (2)
C10—C9—C14—C13−0.7 (3)C34'—N4—C36—C37−69.9 (5)
C8—C9—C14—C13−178.82 (16)
  7 in total

1.  A highly selective fluorescent chemosensor for Pb2+.

Authors:  Ji Young Kwon; Yun Jung Jang; Yoon Ju Lee; Kwan Mook Kim; Mi Sook Seo; Wonwoo Nam; Juyoung Yoon
Journal:  J Am Chem Soc       Date:  2005-07-20       Impact factor: 15.419

2.  A short history of SHELX.

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

3.  Highly sensitive fluorescent probe for selective detection of Hg2+ in DMF aqueous media.

Authors:  Dayu Wu; Wei Huang; Chunying Duan; Zhihua Lin; Qingjin Meng
Journal:  Inorg Chem       Date:  2007-02-01       Impact factor: 5.165

4.  2-[(5-Chloro-2-hy-droxy-benzyl-idene)amino]-3',6'-bis-(diethyl-amino)-spiro-[isoindoline-1,9'-xanthen]-3-one.

Authors:  Zhi-Hong Xu; Wei-Yun Guo; Bo-Wei Su; Xu-Ke Shen; Feng-Ling Yang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-05-29

5.  [(2-{[3',6'-Bis(ethyl-amino)-2',7'-dimethyl-3-oxospiro-[1H-isoindole-1,9'-9H-xanthen]-2-yl}eth-yl)amino-meth-yl]phenol.

Authors:  Li-Zhu Zhang; Xiao-Jun Peng; Shang Gao; Jiang-Li Fan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-01-09

6.  2-[(2,4-Dihydroxy-benzyl-idene)amino]-3',6'-bis-(ethyl-amino)spiro-[isoindoline-1,9'-xanthen]-3-one.

Authors:  Zhi-Hong Xu; Yan-Ling Zhang; Yan-Ru Zhao; Feng-Ling Yang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-05-29

7.  3',6'-Bis(ethyl-amino)-2-[(2-hydroxy-ethyl)-amino]-2',7'-dimethylspiro-[isoindoline-1,9'-xanthen]-3-one.

Authors:  Mao-Zhong Tian; Xiao-Jun Peng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-07-31
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.