Table of Contents Author Guidelines Submit a Manuscript
Bioinorganic Chemistry and Applications
Volume 2010 (2010), Article ID 281932, 8 pages
Research Article

Synthesis, X-Ray Structure, and Characterization of Catena-bis(benzoate)bis{N,N-bis(2-hydroxyethyl)glycinate}cadmium(II)

1Department of Chemistry, University of Patras, 265 04 Patras, Greece
2Institute of Materials Science, NCSR “Demokritos”, 153 10 Aghia Paraskevi Attikis, Greece

Received 20 May 2010; Accepted 12 July 2010

Academic Editor: E. R. Milaeva

Copyright © 2010 Eugenia Katsoulakou et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The reaction of -bis(2-hydroxyethyl)glycine (bicine; ) with in MeOH yielded the polymeric compound . The complex crystallizes in the tetragonal space group . The lattice constants are and  Å. The compound contains chains of repeating units. One atom is coordinated by two carboxylate oxygen, four hydroxyl oxygen, and two nitrogen atoms from two symmetry-related 2.21111 (Harris notation) ligands. The other atom is coordinated by six carboxylate oxygen atoms, four from two ligands and two from the monodentate benzoate groups. Each bicinate(-1) ligand chelates the 8-coordinate, square antiprismatic atom through one carboxylate oxygen, the nitrogen, and both hydroxyl oxygen atoms and bridges the second, six-coordinate trigonal prismatic center through its carboxylate oxygen atoms. Compound 1 is the first structurally characterized cadmium(II) complex containing any anionic form of bicine as ligand. IR data of 1 are discussed in terms of the coordination modes of the ligands and the known structure.

1. Introduction

There are many areas illustrating the importance of cadmium coordination and bioinorganic chemistry and the need for further research in this field. The mobilization and immobilization of in the environment, in the organisms, and in some technical processes can depend significantly on the complexation by chelating organic ligands [1]. For example, anthropogenic chelators released into the environment, humic acids, and several types of ligands produced by microorganisms contribute to the transfer of this metal ion between solid and aqueous phases [2]. Examples of applied cadmium coordination chemistry are found in wastewater treatment and organic separation problems [1, 3]. Cadmium is also important in the interdisciplinary field of Bioinorganic Chemistry. Though probably does not have any biological function, the body of a normal human adult usually contains some milligrams of it [4], mainly in metallothioneins, where it is tightly bonded to cysteinyl sulfur atoms [5]. In special cases of cadmium poisoning, the so-called “chelation therapy” can be applied in which synthetic chelators, like and 2,3-dimercapto-1-propanol (BAL), are given as antidotes [6]. A number of research groups have been also using 113Cd NMR spectroscopy as a “spin spy” in the study of -containing proteins [7]. Systematic comparative studies on the coordination chemistry of and with ligands containing donor groups of biological relevance are useful in this topic. The stereochemical adaptability of this d10 metal ion favours structural variations, and this fact makes a central “player” in the fields of Crystal Engineering and Metallosupramolecular Chemistry [8, 9].

Amongst the ligands that have never been used for the preparation and study of complexes, neither in the solid state nor in solution, is N,N-bis(2-hydroxyethyl)glycine, generally known as bicine (bicH3, Scheme 1). This is a currently “hot” ligand in Bioinorganic Chemistry. Bicine was first prepared in 1926 by Kiprianov and subsequently became a widely used buffer substance in many biochemical studies [11]. As with its parent compound, the amino acid glycine (glyH) also shown in Scheme 1, the monoanion of bicine, that is, the bicinate (−1) ion (), forms metal complexes. The stability constants of many divalent transition metal complexes of bicinate (−1) have been determined, and it has been found that the [M(bicH2)]+ species is always the predominant species in solution [12]. It has repeatedly emphasized [1315] that as a consequence of its strong complexation properties, the use of bicine as a pH buffer in biochemical or medical studies under the assumption that only little (or no) interaction with divalent metal ions occurs is not justified. It has been shown that not only do bicH3 and related compounds buffer H+ concentrations but also the resultant metal complexes buffer H+ and metal ion concentrations; therefore the employment of bicH3 as a buffer requires great care to avoid conflicting data and erroneous conclusions [1315]. Even though bicinate metal complexes have been studied in solution for years [1218], mainly through the excellent research of Sigel [12], only few metal complexes have been structurally characterized in the solid state through single-crystal, X-ray crystallography. In those structural studies it was found (see “Results and Discussion”) that the anionic , , and ligands are versatile and behave in a variety of terminal and bridging modes. Due to this versatility, the anionic forms of bicine are promising ligands for the isolation of polynuclear transition metal complexes (clusters) [19, 20]. Transition metal cluster chemistry is a currently “hot” research field in contemporary inorganic chemistry [21].

Scheme 1: Formulae of N,N-bis(2-hydroxyethyl)glycine (bicine; bicH3) and glycine (glyH) discussed in the paper.

In this paper we report the amalgamation of the above-mentioned two research areas by reporting the preparation, structural characterization, and spectroscopic study of the first cadmium(II) bicinate complex. This paper can be considered as a continuation of our interest in the coordination chemistry of bicine [11] and in the carboxylate chemistry [22].

2. Experiments

All manipulations were performed under aerobic conditions using materials and solvents as received. Cd(O2CPh)22H2O was prepared by the reaction of Cd(O2CMe)22H2O with an excess of PhCO2H in CHCl3 under reflux. C, H, and N analyses were performed with a Carlo Erba EA 108 analyzer. IR spectra (400–450 cm-1) were performed with a Perkin-Elmer PC16 FT-IR spectrometer with samples prepared as KBr pellets.

Solid bicH3 (0.120 g, 0.74 mmol) was added to a colourless solution of Cd(O2CPh)22H2O (0.289 g, 0.74 mmol) in MeOH (40 cm3); the solid soon dissolved. The solution was refluxed for 20 min and allowed to slowly evaporate at room temperature. Well-formed, X-ray quality colourless crystals of the product appeared within a period of three days. The crystals were collected by vacuum filtration, washed with cold MeOH ( cm3) and Et2O ( cm3), and dried in air. The yield was ca. 75%. Found %: C, 39.12; H, 3.97; N, 3.50. Calc % for C26H34N2O12Cd2: C, 39.46; H, 4.34; N, 3.54. IR data (KBr, cm-1): 3235 (sb), 3070 (mb), 2972 (m), 2940 (w), 2894 (w), 1606 (s), 1582 (s),1490 (w), 1445 (w), 1418 (m), 1384 (s), 1334 (m), 1264 (m), 1237 (m), 1174 (w), 1157 (w), 1138 (m), 1069 (s), 1017 (s), 992 (w), 943 (m), 885 (s), 846 (m), 797 (w), 727 (s), 608 (m), 584 (m), 552 (w).

2.1. X-ray Crystallography

X-ray data were collected at 298 K using a Crystal LOGIC dual Goniometer diffractometer with graphite-monochromated radiation ( Å). The appropriate crystal was mounted in air and covered with epoxy glue. Unit cell dimensions were determined and refined by using the angular settings of 25 automatically centered reflections in the range . Intensity data were recorded using a θ–2θscan. Three standard reflections showed less than 3% variation and no decay. Lorentz polarization and -scan absorption corrections were applied using Crystal Logic software. The structure was solved by direct methods using SHELXS-97 [23] and refined by full-matrix least-squares techniques on with SHELX-97 [24]. Hydrogen atoms were located by difference maps and refined isotropically, except those on O(3), C(6), and C(15) which were introduced at calculated positions as riding on bonded atoms with U equal 1.3 times the U(eq) of the respective atom. All nonhydrogen atoms were refined anisotropically. CCDC 771321 contains the supplementary crystallographic data for this paper. This data can be obtained free of charge at [or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: ++44-1223-336 033; E-mail:]. Important crystal data and parameters for data collection and refinement are listed in Table 1.

Table 1: Crystal data and structure refinement for complex 1.

3. Results and Discussion

3.1. Synthetic Comments

Treatment of bicH3 with 1.5 equivalent of Cd(O2CPh)22H2O in refluxing MeOH gave a colourless solution from which complex was obtained in 60% yield (based on the ligand). Its formation can be represented by the stoichiometric equation

The “wrong” to bicH3 reaction ratio (1.5 : 1) employed for the preparation of 1 did not prove detrimental to the formation of the product. With the identity of 1 established by single-crystal X-ray crystallography, the “correct” stoichiometry (1 : 1) was employed and led to the pure compound in 75% yield (see Section 2).

The PhCO2- group present in the reaction mixture plays a double role. It helps the deprotonation of bicH3 and participates in the complex as ligand.

As a next step we decided to use a large excess of Cd(O2CPh)22H2O ( : bicH3 = 3 : 1) or to add base (LiOH, Et3N, ) in the reaction mixture targeting the double or/and triple deprotonation of bicine. We repeatedly isolated a powder, analyzed as Cd2(O2CPh)(bic)(H2O)2, but we could not crystallize it; thus this second product has yet to be structurally characterized.

3.2. Description of Structure

Selected interatomic distances and angles for complex 1 are listed in Table 2. The molecular structure of the compound is shown in Figure 1.

Table 2: Selected bond lengths (Å) and angles ( for complex 1.
Figure 1: Partially labeled plot of a portion of the chain that is present in complex 1. Single and double primes are used for symmetry-related atoms (see footnote of Table 2).

The compound contains chains of repeating units. Each unit contains two crystallographically independent atoms [Cd, Cd(2)] which lie on crystallographic twofold axes. Cd is coordinated by two carboxylate oxygen atoms [O, O()], four hydroxyl oxygen atoms [O(3), O(4), O(), O()] and two nitrogen atoms [N, N()] from two symmetry-related bicinate(−1), that is, , ligands. Cd(2) is coordinated by six carboxylate oxygen atoms; four of them [O, O(), O(2), O()] belong to two symmetry-related ligands, and two [O(11), O()] come from two symmetry-related monodentate groups. Each simultaneously chelates Cd through one carboxylate oxygen, the nitrogen, and both hydroxyl oxygen atoms forming three stable, 5-membered chelating rings and bridges Cd(2) through its carboxylate oxygen atoms; thus, one carboxylate oxygen atom [O] of is 2. Adopting Harris notation in [10], the crystallographically unique group behaves as a 2.21111 ligand (Scheme 2).

Scheme 2: The to-date crystallographically established coordination modes of the , , and ligands and the Harris notation in [10] that describes these modes.

The Cd- bond distances are in the wide range 2.190(3)–2.550(2) Å. The bridging Cd-O distances [2.373(2), 2.550(2) Å] are asymmetric. The Cd(2)-O bond distance for the bridging bicinate carboxylate oxygen atom is longer than the distance exhibited by the terminal oxygen atom [O(2)] to the same atom [2.550(2) versus 2.311(4) Å]. The increase in bond length upon bridging relative to terminal ligation has been observed previously [22] in complexes containing carboxylate ligands with one bridging oxygen atom. Based on theoretical and experimental studies which have indicated that the syn-lone pairs of the carboxylate group are more basic than the anti-lone pairs [38], one might expect the Cd(2)-O distance to be shorter than the Cd-O distance; however, the reverse relation holds for 1 (see Table 2). This result, which is in accordance with other carboxylate complexes [22], suggests that the Cd-O bond lengths involving  : : 2 carboxylate groups are mainly influenced by geometrical factors rather than the electronic properties of the carboxylate group. The Cd(2)-O bond lengths agree well with values found for other 6-coordinate cadmium(II) carboxylate complexes [39, 40]. The average value for the Cd(2)-O bond distances [2.350(4) Å] is smaller than that for the Cd-O ones [2.435(3) Å], due to the lower coordination of Cd(2) compared to the coordination number of Cd [ versus ]. The intrachain CdCd(2) distance is 4.739(2) Å.

The coordination geometry of Cd(2) can be described as a very distorted trigonal prismatic (Figure 2). The two carboxylate oxygen atoms of and the benzoate oxygen atom constitute each trigonal face. The angles of triangular faces are in the wide range . The two trigonal faces are not parallel, with the planes defined by O-O(2)-O() and O()-O()-O(11) making an angle of . The coordination polyhedron of the donor atoms about Cd is best described as a distorted square antiprism (Figure 3). Since even the more stable of the possible 8-coordinate geometries (square antiprismatic, triangular dodecahedral, and cubic) differ slightly in energy from one another, the geometry observed may be largely a reflection of constraints placed on the complex by ligand requirements and packing considerations.

Figure 2: The distorted trigonal prismatic geometry of Cd(2) in complex 1. Double primes are used for symmetry-related atoms (see footnote of Table 2).
Figure 3: The distorted square antiprismatic stereochemistry about Cd in complex 1. The coordination bonds have not been drawn for clarity. Primes are used for symmetry-related atoms (see footnote of Table 2).

Compound 1 is hydrogen bonded. Metric parameters for the bonds are listed in Table 3. The O-HO hydrogen bonds are intrachain. Both hydroxyl oxygen atoms [O(3), O(4)] are involved as donors, while both the coordinated [O(11)] and uncoordinated [O(12)] benzoate oxygen atoms act as acceptors. A weak interchain hydrogen bond, involving one benzoate carbon atom [C(16)] as donor and the terminally ligated carboxylate oxygen atom [O(2)] of a ligand from a neighbouring chain as acceptor, is responsible for the formation of a 2D network.

Table 3: Dimensions of the hydrogen bonds (distances in Å and angles in ) for complex 1.

Compound 1 joins a family of mononuclear, polynuclear, and polymeric complexes with the mono- (), di- (), and trianionic (bic3-) derivatives of bicine as ligands [11, 19, 20]. The members of this family are listed in Table 4, together with the coordination modes of the bicinate ligands for convenient comparison. The to-date crystallographically established coordination modes of , , and bic3- are shown in Scheme 2. Compound 1 is the first cadmium(II) bicinate complex which has been structurally characterized. The ligand in 1 adopts the extremely rare coordination mode 2.21111; see Scheme 2. This ligation mode has been observed in the past only in the 1D coordination polymer Mn2(bicH2)2(H2O)2]Br22H2O [36], in which the ions are 7 coordinate with a slightly distorted pentagonal bipyramidal coordination geometry.

Table 4: Formulae and coordination modes of the bicinate groups of the structurally characterized metal complexes containing various forms of bicine as ligands.
3.3. IR Spectroscopy

IR assignments of selected diagnostic bands for bicH3 (the free ligand exists in its zwitterionic form in the solid state with the carboxylic group being deprotonated and the tertiary nitrogen atom protonated [41]) and complex 1 are given in Table 5.

Table 5: Most characteristic and diagnostic IR fundamentals (cm-1) for bicH3 and complex 1.

The IR spectrum of complex 1 exhibits a medium intensity, broad band at 3070 cm-1, attributable to the O-H stretching vibration of the bicinate() ligand [11, 27, 28]. The broadness and low frequency of this band are both indicative of strong hydrogen bonding [11]. The mode is situated at lower frequencies in the spectrum of 1 than for free bicH3 (at 3190 and 3090 cm-1 [28]); this shift is consistent with the coordination of the –OH groups. The and bands of 1 appear at 1582 and 1418 cm-1 [11]. The corresponding bands of free, zwitterionic bicH3 are at 1639 and 1401 cm-1 [28, 29]. The fact that (164 cm-1) (238 cm-1), where , is in accordance with the crystallographically established chelating-bridging mode (::) of the bicinate() carboxylate group [42]. The strong bands at 1606 and 1384 cm-1 in the spectrum of 1 are assigned to the (CO2) and (CO2) modes of the benzoate ligands, respectively [42]. The parameter is 222 cm-1 significantly larger than that for NaO2CPh (184 cm-1), as expected for the monodentate mode of benzoate ligation [42].

4. Conclusions and Perspectives

Complex 1 covers a gap in literature, because it is the first structurally characterized cadmium(II) bicinate compound. The bicinate() ligand adopts the extremely rare pentadentate 2.21111 coordination mode, while the two crystallographically independent centers are found in two different stereochemistries.

The results presented here support our belief that the bic   ligand “blends” may be effective generators of interesting structural types in the chemistry of other transition metals. Reactions of CdCl2, CdBr2, CdI2, and Cd(NO3)2 with bicH3 have not been studied to date, and we do believe that the structural types of the products will be dependent on the particular nature of the source. Analogues of 1 with zinc(II) have not yet been reported, but preliminary results in our laboratories indicate completely different chemistry compared with that of cadmium(II). Synthetic efforts are also in progress to “activate” the potential of and bic3- to bridge more than four metal ions.


  1. H. Strasdeit, W. Saak, S. Pohl, W. L. Driessen, and J. Reedijk, “Synthetic and structural studies on the novel nitrogen ligand 2,5,8,10,13,16-Hexaazapentacyclo[,5.09,18013,17]octadecane and its reaction products with methanolic cadmium halogenide solutions: Ci-C12H22N6, [CdX2(Ci-C12H22N6)] (X=Cl, Br, I), and [CdI2(C12H23N6OCH3)],” Inorganic Chemistry, vol. 27, no. 9, pp. 1557–1563, 1988. View at Google Scholar · View at Scopus
  2. U. Förstner and G.T.W. Wittmann, Metal Pollution in the Aquatic Environment, Springer, Berlin, Germany, 1983.
  3. S. K. Sahni and J. Reedijk, “Coordination chemistry of chelating resins and ion exchangers,” Coordination Chemistry Reviews, vol. 59, no. C, pp. 1–139, 1984. View at Google Scholar · View at Scopus
  4. L. Friberg, C.-G. Elinder, T. Kjellström, and G. F. Nordberg, Eds., Cadmium and Health: A Toxicological and Epidemiological Appraisal, vol. 1, CRC, Boca Raton, Fla, USA, 1985.
  5. J. H. R. Kägi and M. Nordberg, Metallothionein, Birkhäuser, Basel, Switzerland, 1979.
  6. R. E. Gosselin, R. P. Smith, H. C. Hodge, and J. E. Braddock, Clinical Toxicology of Commercial Products, Williams and Wilkins, Baltimore, Md, USA, 1984.
  7. D. L. Reger, J. E. Collins, S. M. Myers, A. L. Rheingold, and L. M. Liable-Sands, “Syntheses of cationic, six-coordinate cadmium(II) complexes containing tris(pyrazolyl)methane ligands. Influence of charge on cadmium-113 NMR chemical shifts,” Inorganic Chemistry, vol. 35, no. 17, pp. 4904–4909, 1996. View at Google Scholar · View at Scopus
  8. Z. Wang, R.-G. Xiong, B. M. Foxman, S. R. Wilson, and W. Lin, “Two- and three-dimensional cadmium coordination polymers based on N,N-(2-pyridyl)-(4-pyridylmethyl)amine,” Inorganic Chemistry, vol. 38, no. 7, pp. 1523–1528, 1999. View at Google Scholar · View at Scopus
  9. F. A. Almeida Paz, Y. Z. Khimyak, A. D. Bond, J. Rocha, and J. Klinowski, “Synthesis and characterization of a novel modular cadmium-organic framework with biphenyl-4,4-dicarboxylate,” European Journal of Inorganic Chemistry, no. 11, pp. 2823–2828, 2002. View at Google Scholar · View at Scopus
  10. R. A. Coxall, S. G. Harris, D. K. Henderson, S. Parsons, P. A. Tasker, and R. E. P. Winpenny, “Inter-ligand reactions: in situ formation of new polydentate ligands,” Journal of the Chemical Society, Dalton Transactions, no. 14, pp. 2349–2356, 2000. View at Publisher · View at Google Scholar
  11. A. Messimeri, C. P. Raptopoulou, V. Nastopoulos, A. Terzis, S. P. Perlepes, and C. Papadimitriou, “Synthesis and physical studies of lanthanide(III) complexes of N,N-bis(2-hydroxyethyl)glycinate (bicinate, bicH2-): molecular and crystal structure of [Gd(OM2CMe)(bicH2)(phen)(H2O)](ClO4)·phen·3H2O (phen=1,10-phenanthroline),” Inorganica Chimica Acta, vol. 336, pp. 8–18, Inorganica Chimica Acta. View at Google Scholar
  12. H. Sigel, “Quantification of successive intramolecular equilibria in binary metal ion complexes of N,N-bis(2-hydroxyethyl)glycinate (Bicinate). A case study,” Coordination Chemistry Reviews, vol. 122, no. 1-2, pp. 227–242, 1993. View at Google Scholar
  13. C. R. Krishnamoorthy and R. Nakon, “Free metal ion depletion by Good’s buffers. Bicine 1:1 and 2:1 complexes with Mg(II), Ca(II), Co(II), Ni(II), Cu(II) and Zn(II),” Journal of Coordination Chemistry, vol. 23, pp. 233–243, 1991. View at Google Scholar
  14. N. A. Corfù, B. Song, and J. Liang-nian, “Metal ion/buffer interactions. Stability of binary and ternary metal ion complexes containing the anion of N,N-bis(2-hydroxyethyl)-glycine (bicine) and adenosine 5-triphosphate (ATP),” Inorganica Chimica Acta, vol. 192, no. 2, pp. 243–251, 1992. View at Google Scholar
  15. L.-N. Ji, N. A. Corfù, and H. Sigel, “Stability of ternary metal ion complexes formed by imidazole and the anion of N,N-bis(2-hydroxyethyl)glycine (Bicine). Observation of a relatively high stability of the Zn(Bicinate) (imidazole)+ complex,” Inorganica Chimica Acta, vol. 206, no. 2, pp. 215–220, 1993. View at Google Scholar
  16. A. Calderón and A. K. Yatsimirsky, “Formation and phosphodiesterolytic activity of lanthanide(III) N,N-bis(2-hydroxyethyl)glycine hydroxo complexes,” Inorganica Chimica Acta, vol. 357, no. 12, pp. 3483–3492, 2004. View at Publisher · View at Google Scholar
  17. M. Taha, M. M. Khalil, and S. A. Mohamed, “Metal ion-buffer interactions. Complex formation of N,N-bis(2-hydroxyethyl) glycine (Bicine) with various biologically relevant ligands,” Journal of Chemical and Engineering Data, vol. 50, no. 3, pp. 882–887, 2005. View at Publisher · View at Google Scholar
  18. H. A. Azab, K. M. Abou El-Nour, and S. H. Sorror, “Metal ion complexes containing dipeptides, tripeptides, and biologically important zwitterionic buffers,” Journal of Chemical and Engineering Data, vol. 52, no. 2, pp. 381–390, 2007. View at Publisher · View at Google Scholar
  19. M. Murugesu, K. A. Abboud, and G. Christou, “Preparation and properties of new Fe6 and Fe8 clusters of iron(III) with tripodal ligands,” Dalton Transactions, no. 23, pp. 4552–4556, 2003. View at Google Scholar
  20. K. Graham, A. Darwish, A. Ferguson, S. Parsons, and M. Murrie, “Synthesis and characterisation of Fe6 and Fe12 clusters using bicine,” Polyhedron, vol. 28, no. 9-10, pp. 1830–1833, 2009. View at Publisher · View at Google Scholar
  21. A. J. Tasiopoulos and S. P. Perlepes, “Diol-type ligands as central 'players' in the chemistry of high-spin molecules and single-molecule magnets,” Dalton Transactions, no. 41, pp. 5537–5555, 2008. View at Publisher · View at Google Scholar · View at PubMed
  22. T. C. Stamatatos, E. Katsoulakou, V. Nastopoulos, C. P. Raptopoulou, E. Manessi-Zoupa, and S. P. Perlepes, “Cadmium carboxylate chemistry: preparation, crystal structure, and thermal and spectroscopic characterization of the one-dimensional polymer [Cd(O2CMe)(O2CPh)(H2O)2]n,” Zeitschrift fur Naturforschung, vol. 58, no. 11, pp. 1045–1054, 2003. View at Google Scholar
  23. G. M. Sheldrick, SHELXS-97, Structure Solving Program, University of Göttingen, Göttingen, Germany, 1997.
  24. G. M. Sheldrick, SHELXL-97, Crystal Structure Refinement Program, University of Göttingen, Göttingen, Germany, 1997.
  25. N. N. Anan'eva, N. I. Samus, T. N. Polynova, M. A. Porai-Koshits, and N. D. Mitrofanova, “Crystal structure of the divalent copper-diethanoglycine complex,” Journal of Structural Chemistry, vol. 16, no. 3, pp. 480–481, 1975. View at Google Scholar
  26. H. Thakuria and G. Das, “CuO micro plates from a 3D metallo-organic framework (MOF) of a binary copper(II) complex of N,N-bis(2-hydroxyethyl)glycine,” Polyhedron, vol. 26, no. 1, pp. 149–153, 2007. View at Publisher · View at Google Scholar
  27. E. B. Chuklanova, T. N. Polynova, M. A. Porai-Koshits, and G. K. Babeshkina, “Crystal structure of bis[N,N-di(hydroxyethyl)glycinato]nickel,” Soviet Journal of Coordination Chemistry, vol. 7, pp. 459–463, 1981. View at Google Scholar
  28. H. Yamaguchi, M. Nagase, Y. Yukawa, Y. Inomata, and T. Takeuchi, “Synthesis, properties, and crystal and molecular structure of chloro[N,N-bis(2-hydroxyethyl)glycinato]copper(II),” Bulletin of the Chemical Society of Japan, vol. 61, pp. 2763–2766, 1988. View at Google Scholar
  29. H. Yamaguchi, Y. Inomata, and T. Takeuchi, “Synthesis, properties, and crystal and molecular structure of N,N-bis(2-hydroxyethyl)glycinato copper(II) perchlorate monohydrate,” Inorganica Chimica Acta, vol. 161, no. 2, pp. 217–221, 1989. View at Google Scholar
  30. H. Yamaguchi, Y. Inomata, and T. Takeuchi, “Synthesis, properties and crystal and molecular structure of isothiocyanato [N,N-bis(2-hydroxyethyl)glycinato] copper(II) monohydrate,” Inorganica Chimica Acta, vol. 172, no. 1, pp. 105–108, 1990. View at Google Scholar
  31. H. Yamaguchi, Y. Inomata, and T. Takeuchi, “Syntheses, properties, and crystal and molecular structures of bromo[N,N-bis(2-hydroxyethyl)glycinato]copper(II) and aquabromo[N,N-bis(2-hydroxyethyl)glycinato]copper(II),” Inorganica Chimica Acta, vol. 181, no. 1, pp. 31–36, 1991. View at Google Scholar
  32. Z. Sun, P. K. Gantzel, and D. N. Hendrickson, “One-dimensional polymeric bicinate manganese complex,” Polyhedron, vol. 16, no. 19, pp. 3267–3271, 1997. View at Google Scholar
  33. Z. Sun, P. K. Gantzel, and D. N. Hendrickson, “Zigzag chain of hepta-coordinate manganese complexes,” Polyhedron, vol. 17, no. 9, pp. 1511–1516, 1998. View at Google Scholar
  34. X.-F. He, L.-S. Long, X.-Y. Le, X.-M. Chen, L.-N. Ji, and Z.-Y. Zhou, “Solid and solution studies of ternary copper(II) complexes formed by heteroaromatic N bases and the anion of N,N-bis(2-hydroxyethyl)glycine (bicine),” Inorganica Chimica Acta, vol. 285, no. 2, pp. 326–331, 1999. View at Google Scholar
  35. Y. Inomata, T. Takei, and F. S. Howell, “Synthesis and crystal structure of lanthanide metal complexes with N,N-bis(2-hydroxyethyl)glycine,” Inorganica Chimica Acta, vol. 318, no. 1-2, pp. 201–206, 2001. View at Publisher · View at Google Scholar
  36. A. M. Kirillov, M. Haukka, M. Fátima, M. F. C. G. Da Silva, and A. J. L. Pombeiro, “Preparation and crystal structures of benzoylhydrazido- and -diazenidorhenium complexes with N,O-ligands and their catalytic activity towards peroxidative oxidation of cycloalkanes,” European Journal of Inorganic Chemistry, no. 11, pp. 2071–2080, 2005. View at Publisher · View at Google Scholar
  37. A. M. Kirillov, M. Haukka, M. V. Kirillova, and A. J. L. Pombeiro, “Single-pot ethane carboxylation catalyzed by new oxorhenium(V) complexes with N,O ligands,” Advanced Synthesis and Catalysis, vol. 347, no. 10, pp. 1435–1446, 2005. View at Publisher · View at Google Scholar
  38. K. B. Wiberg and K. E. Laidig, “Barriers to rotation adjacent to double bonds. 3. The C-O barrier in formic acid, methyl formate, acetic acid, and methyl acetate. The origin of ester and amide "resonance",” Journal of the American Chemical Society, vol. 109, no. 20, pp. 5935–5943, 1987. View at Google Scholar
  39. X.-L. Wang, C. Qin, E.-B. Wang, Z.-M. Su, and Z.-M. Su, “Metal nuclearity modulated four-, six-, and eight-connected entangled frameworks based on mono-, Bi-, and trimetallic cores as nodes,” Chemistry-A European Journal, vol. 12, no. 10, pp. 2680–2691, 2006. View at Publisher · View at Google Scholar · View at PubMed
  40. Q.-R. Fang, G.-S. Zhu, M. Xue, J.-Y. Sun, and S.-L. Qiu, “Porous coordination polymers with zeolite topologies constructed from 4-connected building units,” Dalton Transactions, no. 20, pp. 2399–2402, 2006. View at Publisher · View at Google Scholar · View at PubMed
  41. V. Cody, J. Hazel, and D. A. Langs, “N,N-bis(2-hydroxyethyl)glycine,” Acta Crystallographica B, vol. 33, pp. 905–907, 1977. View at Google Scholar · View at Scopus
  42. G. B. Deacon and R. J. Phillips, “Relationships between the carbon-oxygen stretching frequencies of carboxylato complexes and the type of carboxylate coordination,” Coordination Chemistry Reviews, vol. 33, pp. 227–250, 1980. View at Google Scholar