Electroproduction of π0-mesons on protons at very low values of |q 2|

The electroproduction of π⁰-mesons on protons has been measured with electrons of 1.7 and 2.1 GeV energy in the region of the nucleon resonances at \(W = \sqrt {(q + p)^2 } = 1,400 - 2,000MeV\) at rather low values of |q ²|=|(e?e′)²|=0.01–0.1 GeV² but at high values of the nucleon recoil |t|=|(p?p′)²|≈0.6–2.2 GeV² corresponding to \(\Theta _\pi ^{cm} \approx 145^ \circ - 180^ \circ\) . Up toW≈1,650 MeV the cross section for π⁰-production with virtual photons of |q ²|≈0.03 GeV² is only slightly smaller than that with real photons. ForW?1,700 MeV the cross section at |q ²|≈0.03 GeV² is on average a factor of 2 smaller than that atq ²=0 but only slightly higher than that at |q ²|≈0.3–1 GeV².     

Novel UDP-glycal derivatives as transition state analogue inhibitors of UDP-GlcNAc 2-epimerase

The "epimerisation" of UDP-GlcNAc to ManNAc, the first step in the biosynthesis of sialic acids, is catalyzed by UDP-GlcNAc 2-epimerase. In this paper we report the synthesis of transition state based inhibitors of this enzyme. To mimic the assumed first transition state of this reaction (TS 1), we designed and synthesized the novel UDP-exo-glycal derivatives 1-4. We also report herein the synthesis of 5 and 6, the first C-glycosidic derivatives of 2-acetamidoglucal, and the synthesis of the ketosides 7 and 8, which were designed as bis-substrate analogue and bis- product analogue, respectively, to mimic the second step of the reaction via the assumed second transition state TS 2.     

Study of the properties of the SHG with diode lasers

An experimental study of the second-harmonic generation (SHG) properties with nondiffraction-limited radiation is presented. This includes the dependency of the normalized conversion efficiency on the crystal length, the beam quality, and the focusing conditions. A Gauss–Schell-model-based theory of SHG is applied, which gives an improved simulation of the experimental results in comparison to the standard Boyd–Kleinman theory for nondiffraction-limited beams.     

The Role of 2,6‐Diaminopyridine Ligands in the Isolation of an Unprecedented,Low‐Valent Tin Complex

Stabilization of the central atom in an oxidation state of zero through coordination of neutral ligands is a common bonding motif in transition‐metal chemistry. However, the stabilization of main‐group elements in an oxidation state of zero by neutral ligands is rare. Herein, we report that the transamination reaction of the DAMPY ligand system (DAMPY=2,6‐[ArNH‐CH₂]₂(NC₅H₃) (Ar=C₆H₃‐2,6‐iPr₂)) with Sn[N(SiMe₃)₂]₂ produces the DIMPYSn complex (DIMPY=(2,6‐[ArN?CH]₂(NC₅H₃)) with the Sn atom in a formal oxidation state of zero. This is the first example of a tin compound stabilized in a formal oxidation state of zero by only one donor molecule. Furthermore, three related low‐valent Sn^II complexes, including a [DIMPYSn^IICl]⁺[SnCl₃]^? ion pair, a bisstannylene DAMPY{Sn^II[N(SiMe₃)₂]₂}₂, and the enamine complex MeDIMPYSn^II, were isolated. Experimental results and the conclusions drawn are also supported by theoretical studies at the density functional level of theory and ¹¹⁹Sn Mössbauer spectroscopy.