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  • 1
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: 2,3-Diketopiperazine (2,3-piperazinedione), C4H6N2O2, crystallizes in the monoclinic space group P21/c with a = 5.941 (3), b = 10.080 (3), c = 8.282 (2) Å, β = 95.87 (3)°, V = 493.4 (5) Å3, Z = 4, Dx = 1.536 Mg m−3 and Mr = 114.1. The six-membered ring adopts a skew-boat conformation with Q = 0.467 (3) Å, θ = 64.6 (3)° and φ = 269.8 (4)°. The C2 symmetry, which typifies the free molecule, is broken by the formation of two intermolecular N—H...O bonds involving only one of the C=O groups of the 2,3-diketopiperazine molecule. The intensity data typical for a time series are summarized in traditional statistics by B = σ2(B) = ΣBi and R = σ2(R) = ΣRi, where B is the background and R the raw intensity. Exploitation of the same data using Bayesian methodology leads to similar values for B and R, but the variances for these signals are significantly smaller. This reduction in variance is dictated by the length N of the time series. With 25 observations in each hkl time series we arrive at variances that are 25% of their classical values. So, a measuring strategy in which a single observation with a slow scan at speed 1/N is preferred above a series of N observations at speed 1 produces the worst possible benefit within a fixed time frame. In complete contrast to our expectation, structure refinements reveal that that the standard deviation of an observation of unit weight, S, will converge towards its ideal unit value only when we decrease the accuracy of the data set. This unpleasant behaviour points to a serious discrepancy between accuracy and precision. Our reflection intensities are systematically wrong, because we underestimate the wavelength dispersion. On our CAD-4 equipment a sealed Mo tube and the standard graphite monochromator produce an incident beam with Δλ/λ = 14%. As a consequence, the observed background intensities are not representative of the real background. The size of the background error depends on the nearby Bragg intensity. The magnitude of the signal pollution contaminating the local background is ∼2% of the maximum Bragg intensity found at λ = 0.71 Å.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 54 (1998), S. 859-865 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: 2,3-Diketopiperazine (2,3-piperazinedione) crystallizes in the monoclinic space group P21/c with a = 5.941 (3), b = 10.080 (3), c = 8.282 (2) Å and β = 95.87 (3)°. The six-membered ring adopts a skew-boat conformation with Q = 0.467 (3) Å, θ = 64.6 (3)° and φ = 269.8 (4)°. Ab initio calculations show that the perfect skew-boat with its C2 symmetry is broken by the formation of two intermolecular N—H...O bonds, involving only one of the C=O groups of the 2,3-diketopiperazine molecule. Vibrational spectra were recorded in solution and in the solid state. The assignment of the normal vibrations is proposed based on comparison with spectra of similar molecules and spectral changes due to deuteration. Ab initio calculations for the isolated molecule and the solid-state structure were used to calculate differences in the molecular geometry in the gas phase and crystalline state. Using these reference structures we calculated the stretching frequencies for the C=O groups. We predict an IR shift for C=O of 130 cm−1, when the molecule goes from the gas phase to the solid state. The observed shift is 110 cm−1. The differences between the C=O moieties in the solid state produce a calculated Δν of 55 cm−1, which matches satisfactorily the observed value of 49 cm−1.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 47 (1996), S. 135-142 
    ISSN: 1572-8943
    Keywords: complexes ; IR ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Dithiomalonamide [H2A, CH2(CSNH2)2] and 2,2-dimethyldithiomalonamide [H2B, C(CH3)2(CSNH2)2] can act as bidentate ligands and form stable, cationic 1∶2 complexes with general formula M2(H2L)2X2 [M=Ni2+, Pd2+, Pt2+;X=C1, Br, I; H2L=H2A, H2B] in strong acidic medium. An elaborate thermal study is presented, based on results from elemental analyses and vibrational studies (IR and Raman spectroscopy). The H2A complexes start to decompose by releasing two HX molecules whereafter a stable intermediate M(HA)2 is formed. The H2B complexes degrade in a different way; the metal-sulphur bond is broken and the ligand is expelled as a whole. Influences of the metal ion and of the halogenide counterions are investigated.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 47 (1996), S. 143-150 
    ISSN: 1572-8943
    Keywords: complexes ; oxathioamidate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Oxathioamidates (CSNR1 R 2COOKR 1=R 2=H (A),R 1=H andR 2=CH3 (B),R 1,=R 2=CH3 (C)) can act as O, S donors and form pentaatomic ring systems with divalent metals (M(II)=Mn, Fe, Co, Ni, Cu, Zn). Vibrational spectra and thermal analysis provide information on the amount and nature of associated water molecules. The dehydration of MA2(H2O)2 (M=Mn, Fe, Co, Ni) can be very well explained by the C.F.S.E. (crystal field stabilization energy) for weak field octahedral complexes. The complexes with ligand A and B decompose to form polymers by deprotonation on the thioamide group. The proposed structures are confirmed by the vibrational spectra. For ligand C no stable intermediates are formed during heating, degradation proceeds until metal sulphide remains.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 48 (1997), S. 225-231 
    ISSN: 1572-8943
    Keywords: activation energy ; amides ; enthalpy of sublimation ; hydrogen bonding ; thioamides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of intermolecular hydrogen bonding on some physical constants is clearly shown by comparing some thermal data for simple oxamides and thiooxamides.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 284-288 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The barrier to the internal rotation of the dimethylamino group in thioamides of structure R—CS—N(CH3)2, R being (CH3)2,N—CS—, CH3O2C— or N≡C—, is studied by proton magnetic resonance, using the lineshape analysis method of Nakagawa. In the solvents o-dichlorobenzene, naphthalene and nitrobenzene all ΔG≠ values are in the range of 23 to 24 kcal/mol. In these solvents the Ea and ΔS≠ values of each product are linearly related to the dielectric constants.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 279-283 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical shifts of the N-methyl signals for a number of thio-oxamide and oxamide derivatives are unambiguously determined in the solvents chloroform, carbon tetrachloride, benzene, chlorobenzene, o-dichlorobenzene and nitrobenzene. The ASIS effect is discussed. The temperature dependence of the absolute shift and of the relative shift differences of both methyl groups of the N,N-dimethyl derivatives are studied.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 26 (1995), S. 77-82 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman and infrared measurements were performed on hydrated (H2O and D2O) and anhydrous (CH3)2NCSCOOK together with their CD3-substituted analogues. Close scrutiny of the water fundamentals indicated that the C2v symmetry of the single water molecule is lost owing to different strengths of hydrogen bonding with the carboxylate and thioamide functional groups. The number of water fundamentals and the wavenumber and intensity changes at different temperatures are, considering the very complex structure of the water spectra, unexpectedly consistent with the predictions of a single asymmetric water molecule.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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