2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate

Bulatov, Evgeny; Boyarskaya, Dina; Chulkova, Tatiana; Haukka, Matti

doi:10.1107/S1600536814002372

Publisher's PDF

Katso/Avaa

337.3 Kb

Lataukset:

Show download details Hide download details

Bulatov, E., Boyarskaya, D., Chulkova, T., & Haukka, M. (2014). 2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate. Acta Crystallographica Section E : Structure Reports Online, 70(3), o260. https://doi.org/10.1107/S1600536814002372

Julkaistu sarjassa

Acta Crystallographica Section E : Structure Reports Online

Tekijät

Bulatov, Evgeny |

Boyarskaya, Dina |

Chulkova, Tatiana |

Haukka, Matti

Päivämäärä

2014

Oppiaine

Epäorgaaninen ja analyyttinen kemia Inorganic and Analytical Chemistry

Tekijänoikeudet

In the title compound, C16H11NO2C5H9NO, the dihedral angles between the maleimide and phenyl rings are 34.7 (2) and 64.8 (2). In the crystal, the 2,3-diphenylmaleimide and 1- methylpyrrolidin-2-one molecules form centrosymmetrical dimers via pairs of strong N—HO hydrogen bonds and – stacking interactions between the two neighboring maleimide rings [centroid–centroid distance = 3.495 (2) A˚ ]. The dimers are further linked by weak C—HO and C— H hydrogen bonds into a three-dimensional framework.

Julkaisija

Wiley-Blackwell Publishing, Inc.

ISSN Hae Julkaisufoorumista

1600-5368

Lisenssi

© the Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence.

Ellei muuten mainita, aineiston lisenssi on © the Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence.

Näytetään aineistoja, joilla on samankaltainen nimeke tai asiasanat.

5-Imino-3,4-diphenyl-1H-pyrrol-2-one

Bulatov, Evgeny; Chulkova, Tatiana; Haukka, Matti (Wiley-Blackwell Publishing, Inc., 2014)

The title compound, C16H12N2O, exists in the crystalline state as the 5-imino-3,4-diphenyl-1H-pyrrol-2-one tautomer. The dihedral angles between the pyrrole and phenyl rings are 35.3 (2) and 55.3 (2). In the crystal, ...
Identification of mixed bromidochloridotellurate anions in disordered crystal structures of (bdmim)2[TeX2Y4] (X, Y = Br, Cl; bdmim = 1-butyl-2,3-dimethylimidazolium) by combined application of Raman spectroscopy and solid-state DFT calculations

Närhi, Sari; Kutuniva, Johanna; Lajunen, Marja; Lahtinen, Manu; Tuononen, Heikki; Karttunen, Antti; Oilunkaniemi, Raija; Laitinen, Risto (Elsevier B.V., 2014)

The discrete mixed [TeBrxCl6−x]2− anions in their disordered crystal structures have been identified by using the phases prepared by the reaction of 1-butyl-2,3-dimethylimidazolium halogenides (bdmim)X with tellurium ...
Structural, Thermoanalytical and Molecular Modeling Studies on N-(3-hydroxypropyl) 3a,12a-Dihydroxy-5b-cholan-24-amide and Its Monohydrates

Valkonen, Arto; Kolehmainen, Erkki; Lahtinen, Manu; Sievänen, Elina; Noponen, Virpi; Tolonen, Minna; Kauppinen, Reijo (MDPI, 2007)

The synthetic method for preparing N-(3-hydroxypropyl) 3α,12α-dihydroxy-5β- cholan-24-amide can lead to formation of at least three different crystal forms – an anhydrous compound and two monohydrates. The structural and ...
Structural analysis of two foldamer-type oligoamides – the effect of hydrogen bonding on solvate formation, crystal structures and molecular conformation

Suhonen, Aku; Nauha, Elisa; Salorinne, Kirsi; Helttunen, Kaisa; Nissinen, Maija (RSC Publishing, 2012)

The crystal structures and molecular conformations of two foldamer-type oligoamides were analyzed. One polymorphic form and seven solvates were found for N¹,N³-bis(2-benzamidophenyl)benzene-1,3-dicarboxamide (the benzene ...
Crystal Structures and Density Functional Theory Calculations of o-and p-Nitroaniline Derivatives: Combined Effect of Hydrogen Bonding and aromatic interactions on dimerization energy

Helttunen, Kaisa; Lehtovaara, Lauri; Häkkinen, Hannu; Nissinen, Maija (American Chemical Society, 2013)

The interplay of strong and weak hydrogen bonds, dipole–dipole interactions, and aromatic interactions of o- and p-nitroaniline derivatives was studied by combining crystal structure analysis and density functional theory ...