Polysulfonylamine, CLVII [1]. Molekulare Cokristalle aus Di(4-halogenbenzolsulfonyl)aminen und Sauerstoffbasen: Lamellare Schichten mit engen Zwischenschichtkontakten der Art C-H···Hal, Cl ··· Cl oder Br ··· Br / Molecular Co-crystals of Di(4-halobenzenesulfonyl)amines and Oxygen Bases: Lamellar Layers with Close C-H···Hal, Cl · · · Cl or Br · · · Br
-
Thomas Hamann
and
Peter G. Jones
Di(4-fluorobenzenesulfonyl)amine (DFBSA), di(4-chlorobenzenesulfonyl)amine (DCBSA) or di(4-bromobenzenesulfonyl)amine (DBBSA) were co-crystallized with equimolar amounts of pyridine-N-oxide (PyO), dimethyl formamide (DMF) or 1,3-dimethylurea (DMU), respectively, to form the supramolecular complexes DFBSA·PyO (1; triclinic, space group P1 , Z = 1), DCBSA·DMF (2; monoclinic, P21/n, Z = 1) and DBBSA·DMU (3; triclinic, P1 , Z = 1). Throughout the triad, the molecules are ordered into lamellar layers parallel to the xy plane. Owing to the folded conformations of the disulfonylamines, the layers display an inner polar region of oxygen bases and (SO2)2NH groups, outer apolar regions of aromatic rings, and interlayer regions hosting the halogen atoms. These arrays mimic the formerly reported structures of a series of ionic metal di(arenesulfonyl)amides. The intralamellar connectivity is governed by conventional hydrogen bonding and weak C-H···O bonds, the former comprising in structure 1 a very strong N-H···O-N interaction [N···O 250,9(2) pm, N-H···O 171(3)°], in 2 an N-H···O=C bond, and in 3 a set of one S2N-H···O=C and two N-H(urea)···O=S bonds. A centrosymmetric (PyO)2 dimer is present in structure 1. The juxtapositions of adjacent layers reflect halogen-specific recognition patterns (1: three short C-H···F sequences, all F···F distances beyond the van der Waals limit dW; 2: one short C-H···Cl sequence and one close Cl ··· Cl contact < dW, all other Cl ··· Cl > dW; 3: four short C-H···Br sequences and one close Br···Br contact < dW, all other Br···Br > dW). The interhalogen contacts in 2 and 3 are of the type I, as characterized by θ(C-X···X')≈ θ(C'-X' ··· X); the four angles θ lie in the range 166-175°
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Articles in the same Issue
- Alkalimetall-Arsenide A3As7 Und Aas (A = K, Rb, Cs). Synthesen, Kristallstrukturen, Schwingungsspektren / Alkaline Metal Arsenides A3As7 and AAs (A = K, Rb, Cs). Preparation, Crystal Structure, Vibrational Spectroscopy
- Synthesen und Kristallstrukturen von Bis(N-lithiumtrimethylsilylamino)- bis(dimethylamino)silan und 1,1-Dichloro-2,4-bis(trimethylsilylamino)- 3,3-bis(dimethylamino)siladiazatitanacyclobutan / Syntheses and Crystal Structures of Bis(N-lithio-trimethylsilylamino)bis(dimethylamino)- silane and 1,1-Dichloro-2,4-bis(trimethylsilylamino)-3,3-bis(dimethylamino)siladiazatitanacyclobutane
- Valence Bond Studies of N5+
- Synthesis and Characterization of Chromium Tricarbonyl Complexes of 1-Phenylgermatrane and 1-Phenylazagermatrane. Crystal Structure of [N(CH2CH2O)3GeC6H5]Cr(CO)3
- Synthesis and Structural Characterization of [Cu(NH2CH2C6H4N=CHC5H5N)Cl2]
- Die Kristallstruktur von Bis-[methylammonium]-hexafluorosilikat, (MeNH3)2SiF6 / The Crystal Structure of Bis-[methylammonium]-hexafluorosilicate, (MeNH3)2SiF6
- New Phosphorus-Containing Polycylic Large-Ring Systems Involving Heteroatoms
- Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Komplexe / Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Complexes
- Zur Reaktion von PCl3 mit NaR*, KR* und ZnR*2 (R* = SitBu3) [1]: Bildung des Diphosphens R*P=PR*, Tetraphosphans P4R*2 , Tetraphosphanids NaP4R*3 sowie von Halogenphosphanen R*mPmClp / On the Reaction of PCl3 with NaR*, KR* and ZnR*2 (R*= SitBu3) [1]: Formation of the Diphosphene R*P=PR*, Tetraphosphane P4R*2, Tetraphosphanide NaP4R*3 as well as Halogenophosphanes R*mPnClp
- Darstellung, Schwingungsspektren und Normalkoordinatenanalyse von (n-Bu4N)2[Pt(SCN)n(ox)], n = 2, 4, sowie Kristallstruktur von [(C5H5N)2CH2][Pt(SCN)4(ox)] / Synthesis, Vibrational Spectra and Normal Coordinate Analysis of (n-Bu4N)2[Pt(SCN)n(ox)], n = 2, 4, and Crystal Structure of [(C5H5N)2CH2][Pt(SCN)4(ox)]
- Hydrothermal Single Crystal Growth and Crystal Structures of the Mercury(II) Selenates(VI) HgSeO4, HgSeO4·HgO and HgSeO4·2HgO
- Polysulfonylamine, CLVII [1]. Molekulare Cokristalle aus Di(4-halogenbenzolsulfonyl)aminen und Sauerstoffbasen: Lamellare Schichten mit engen Zwischenschichtkontakten der Art C-H···Hal, Cl ··· Cl oder Br ··· Br / Molecular Co-crystals of Di(4-halobenzenesulfonyl)amines and Oxygen Bases: Lamellar Layers with Close C-H···Hal, Cl · · · Cl or Br · · · Br
- New Bioactive Diterpenoid from Euphorbia decipiens
- Magnesium Isotope Effects by Ion Exchange Using Monoazacrown Bonded Merrifield Peptide Resin
Articles in the same Issue
- Alkalimetall-Arsenide A3As7 Und Aas (A = K, Rb, Cs). Synthesen, Kristallstrukturen, Schwingungsspektren / Alkaline Metal Arsenides A3As7 and AAs (A = K, Rb, Cs). Preparation, Crystal Structure, Vibrational Spectroscopy
- Synthesen und Kristallstrukturen von Bis(N-lithiumtrimethylsilylamino)- bis(dimethylamino)silan und 1,1-Dichloro-2,4-bis(trimethylsilylamino)- 3,3-bis(dimethylamino)siladiazatitanacyclobutan / Syntheses and Crystal Structures of Bis(N-lithio-trimethylsilylamino)bis(dimethylamino)- silane and 1,1-Dichloro-2,4-bis(trimethylsilylamino)-3,3-bis(dimethylamino)siladiazatitanacyclobutane
- Valence Bond Studies of N5+
- Synthesis and Characterization of Chromium Tricarbonyl Complexes of 1-Phenylgermatrane and 1-Phenylazagermatrane. Crystal Structure of [N(CH2CH2O)3GeC6H5]Cr(CO)3
- Synthesis and Structural Characterization of [Cu(NH2CH2C6H4N=CHC5H5N)Cl2]
- Die Kristallstruktur von Bis-[methylammonium]-hexafluorosilikat, (MeNH3)2SiF6 / The Crystal Structure of Bis-[methylammonium]-hexafluorosilicate, (MeNH3)2SiF6
- New Phosphorus-Containing Polycylic Large-Ring Systems Involving Heteroatoms
- Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Komplexe / Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Complexes
- Zur Reaktion von PCl3 mit NaR*, KR* und ZnR*2 (R* = SitBu3) [1]: Bildung des Diphosphens R*P=PR*, Tetraphosphans P4R*2 , Tetraphosphanids NaP4R*3 sowie von Halogenphosphanen R*mPmClp / On the Reaction of PCl3 with NaR*, KR* and ZnR*2 (R*= SitBu3) [1]: Formation of the Diphosphene R*P=PR*, Tetraphosphane P4R*2, Tetraphosphanide NaP4R*3 as well as Halogenophosphanes R*mPnClp
- Darstellung, Schwingungsspektren und Normalkoordinatenanalyse von (n-Bu4N)2[Pt(SCN)n(ox)], n = 2, 4, sowie Kristallstruktur von [(C5H5N)2CH2][Pt(SCN)4(ox)] / Synthesis, Vibrational Spectra and Normal Coordinate Analysis of (n-Bu4N)2[Pt(SCN)n(ox)], n = 2, 4, and Crystal Structure of [(C5H5N)2CH2][Pt(SCN)4(ox)]
- Hydrothermal Single Crystal Growth and Crystal Structures of the Mercury(II) Selenates(VI) HgSeO4, HgSeO4·HgO and HgSeO4·2HgO
- Polysulfonylamine, CLVII [1]. Molekulare Cokristalle aus Di(4-halogenbenzolsulfonyl)aminen und Sauerstoffbasen: Lamellare Schichten mit engen Zwischenschichtkontakten der Art C-H···Hal, Cl ··· Cl oder Br ··· Br / Molecular Co-crystals of Di(4-halobenzenesulfonyl)amines and Oxygen Bases: Lamellar Layers with Close C-H···Hal, Cl · · · Cl or Br · · · Br
- New Bioactive Diterpenoid from Euphorbia decipiens
- Magnesium Isotope Effects by Ion Exchange Using Monoazacrown Bonded Merrifield Peptide Resin
