Preparation, spectra, and crystal structures of two rhodium(III) complexes with short intramolecular hydrogen bonds

1984 ◽  
Vol 23 (3) ◽  
pp. 330-334 ◽  
Author(s):  
Sutatip Siriparisarnpipat ◽  
E. O. Schlemper
Keyword(s):  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Intramolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen

Heterocyclic Tautomerism. II. 4-Acylpyrazolones. X-Ray Crystal Structures of 4-Benzoyl-5-methyl-2-phenylpyrazol-3(2H)-one and 4-Acetoacetyl-3-methyl-1-phenylpyrazol-5-ol

1985 ◽  
Vol 38 (3) ◽  
pp. 401 ◽  
Author(s):  
MJ O'Connell ◽  
CG Ramsay ◽  
PJ Steel
Keyword(s):  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Room Temperature ◽  
Crystalline Form ◽  
Intermolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen Bonds ◽  
X Ray ◽  
Intramolecular Hydrogen

The colourless crystalline form of the benzoylpyrazolone (2) has molecules with the NH structure (2c) stabilized by intermolecular hydrogen bonds. At room temperature crystals are monoclinic: P21/c, a 13.508(5), b 9.124(4), c 11.451(3)Ǻ, β 90.80(3)°, Z4; the structure was refined to R 0.059, Rw 0.048. The acetoacetylpyrazolone (3) has the OH structure (3c) with two intramolecular hydrogen bonds. At 193 K crystals are triclinic: Pī , a 7.142(2), b 13.704(8), c 14.699(7)Ǻ, α 117.36(3), β 96.87(3), γ 93.73(3)°, Z 4; the structure was refined to R 0.049, Rw 0.054.

Geometric conditions for the formation of short intramolecular hydrogen bonds in dicarboxylic acids and their acid salts. Crystal structures of two cyclopropane derivatives containing such bonds: ammonium hydrogen caronate and potassium hydrogen caronate hydrate

1993 ◽  
Vol 203 (2) ◽  
Author(s):  
H. Küppers ◽  
S. M. Jessen
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Dicarboxylic Acids ◽  
Intramolecular Hydrogen Bonds ◽  
Geometric Conditions ◽  
Ammonium Hydrogen ◽  
Potassium Hydrogen ◽  
Intramolecular Hydrogen ◽  
Cyclopropane Derivatives

Abstract(I) Ammonium hydrogen 3,3-dimethyl-cis-1,2-cyclopropanedicarboxylate (NHBoth compounds show short intramolecular hydrogen bonds with O…O distances of 2.477(5) Å in (I) and 2.425(3) Å in (II). The present structures complement a series of comparable chelate systems. The different geometries in these chelates influence the hydrogen bond lengths (O…O) and produce distortions of the anions to different extents. These considerations, which make the tendency to form

Two phosphonodehydrotripeptides: Boc0–Gly1–Δ(Z)Phe2–α-Abu3PO3Me2and Boc0–Gly1–Δ(Z)Phe2–α-Nva3PO3Et2

2013 ◽  
Vol 69 (3) ◽  
pp. 277-281 ◽  
Author(s):  
Anna Brzuszkiewicz ◽  
Maciej Makowski ◽  
Marek Lisowski ◽  
Elżbieta Lis ◽  
Marta Otręba ◽  
...  
Keyword(s):  
Amino Acids ◽  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Main Chain ◽  
Intermolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen Bonds ◽  
Crystal Forms ◽  
Intramolecular Hydrogen

The present paper reports the crystal structures of two short phosphonotripeptides (one in two crystal forms) containing one ΔPhe (dehydrophenylalanine) residue, namely dimethyl (3-{[tert-butoxycarbonylglycyl-α,β-(Z)-dehydrophenylalanyl]amino}propyl)phosphonate, Boc0–Gly1–Δ(Z)Phe2–α-Abu3PO3Me2, C21H32N3O7P, (I), and diethyl (4-{[tert-butoxycarbonylglycyl-α,β-(Z)-dehydrophenylalanyl]amino}butyl)phosphonate, Boc0–Gly1–Δ(Z)Phe2–α-Nva3PO3Et2, as the propan-2-ol monosolvate 0.122-hydrate, C24H38N3O7P·C3H8O·0.122H2O, (II), and the ethanol monosolvate 0.076-hydrate, C24H38N3O7P·C2H6O·0.076H2O, (III). The crystals of (II) and (III) are isomorphous but differ in the type of solvent. The phosphono group is linked directly to the last Cαatom in the main chain for all three peptides. All the amino acids aretranslinked in the main chains. The crystal structures exhibit no intramolecular hydrogen bonds and are stabilized by intermolecular hydrogen bonds only.

Controlling emissive properties by intramolecular hydrogen bonds: alkyl and aryl meso‐substituted porphycenes

2021 ◽  
Author(s):  
Jacek Waluk ◽  
Arkadiusz Listkowski ◽  
Natalia Masiera ◽  
Michał Kijak ◽  
Roman Luboradzki ◽  
...  
Keyword(s):  
Hydrogen Bonds ◽  
Intramolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen

Energies of intramolecular hydrogen bonds in some alcohols

1974 ◽  
Vol 20 (3) ◽  
pp. 414-415
Author(s):  
Ya. A. Shuster ◽  
V. A. Granzhan ◽  
P. M. Zaitsev
Keyword(s):  
Hydrogen Bonds ◽  
Intramolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen

Hydrogen bonds in derivatives of N-substituted N’-benzoyl- and N’-(2-chlorobenzoyl)thiourea

1991 ◽  
Vol 56 (4) ◽  
pp. 880-885 ◽  
Author(s):  
Oľga Hritzová ◽  
Dušan Koščík
Keyword(s):  
Hydrogen Bonds ◽  
Spectral Studies ◽  
Intramolecular Hydrogen Bonds ◽  
Tautomeric Forms ◽  
Intramolecular Hydrogen ◽  
Derivatives Of

Intramolecular hydrogen bonds of the N-H···O=C type have been detected in the derivatives of N-substituted N’-benzoyl- and N’-(2-chlorobenzoyl)thiourea on the basis of IR spectral studies. The title compounds can exist in two tautomeric forms.

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