2016
DOI: 10.3390/cryst6060069
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Synthesis and Crystal Structures of Two Novel O, N-Containing Spiro Compounds

Abstract: 1187. In 1, there exist some intra-and inter-molecular hydrogen bonds and C-H¨¨¨π supramolecular interactions, while there are still 𨨨π stacking interactions except for some intra-and intermolecular hydrogen bonds in 2. Two compounds both form a three-dimensional network structure via above intermolecular interactions.

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Cited by 9 publications
(10 citation statements)
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“…115.4(2) C(10)−C(15)−C (14) 117.61(2) C(10)−C(15)−C (9) 116.42(2) C(10)−C(15)−C(9) 119.42 (19) The two compounds both consist of a phenyl ring and 6,10-dioxaspiro [4.5]decane-7,9-dione group which connects a five-membered cyclopentane ring with the other O-containing six-membered ring by a C spiro atom (Figure 1). The selected bond lengths and bond angles of compound 1 are similar to those of 2 correspondingly.…”
Section: Compound 1 Compoundmentioning
confidence: 99%
See 1 more Smart Citation
“…115.4(2) C(10)−C(15)−C (14) 117.61(2) C(10)−C(15)−C (9) 116.42(2) C(10)−C(15)−C(9) 119.42 (19) The two compounds both consist of a phenyl ring and 6,10-dioxaspiro [4.5]decane-7,9-dione group which connects a five-membered cyclopentane ring with the other O-containing six-membered ring by a C spiro atom (Figure 1). The selected bond lengths and bond angles of compound 1 are similar to those of 2 correspondingly.…”
Section: Compound 1 Compoundmentioning
confidence: 99%
“…The presence of oxaspirocyclic compounds in various natural products has also emerged, increasing interest due to their important biological activities, such as antimicrobial [9,10], antitumor [11] ,antiproliferative [12], antiviral [13], antiplasmodial [14] and antihistamic [15] activity etc. Based on these reasons, our group began to synthesize various oxaspirocyclic compounds and study their chemical properties [16][17][18][19]. In addition, to the best of our knowledge, oxaspirocyclic compounds derived from 6,10-dioxaspiro [4.5]decane-7,9-dione are very rare.…”
Section: Introductionmentioning
confidence: 99%
“…The structure design methodology and properties of coordination polymers are mainly dependent on the intrinsic organic linkers [9,10], inorganic metal units, as well as the external synthesis conditions such as reaction temperatures, pH of the medium, reaction solvents, and counter anions [11][12][13]. Generally, organic linkers with N and/or O donors have often been utilized as effective building units in the process of coordination polymers [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…Due to their favorable coordination abilities for the N or O donor atoms, the organic linkers incorporating N-heterocyclic bridging or carboxyl groups ligands are extensively applied to construct coordination polymers and have made great progress in the field of crystal engineering [7,8]. The N-heterocyclic bridging ligands include imidazole, triazole, tetrazole, and pyridine or its analogues such as pyridazine, tetrazine, triazine, and pyrazine moieties [9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…It should be noted that numerous intermolecular π-π and C-H···π interactions exist among the aromatic rings, as shown in Figure 3. The benzene rings of the L 1 − ligands between the adjacent 2D layers are parallel and are separated by a centroid-centroid distance of 3.94 Å and C-H···π distance of 3.32 Å [7,19]. The non-classic weak π-π and C-H···π interactions further link the 2D layers into three-dimensional (3D) supramolecular polymer ( Figure 3).…”
Section: Introductionmentioning
confidence: 99%