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Peter Mayer

Bio: Peter Mayer is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Ligand & Denticity. The author has an hindex of 47, co-authored 593 publications receiving 10612 citations. Previous affiliations of Peter Mayer include Humboldt University of Berlin & Nelson Mandela Metropolitan University.


Papers
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TL;DR: In this paper, a new synthesis for 1,5-diamino-1H-tetrazolium nitrate (2a) and perchlorate (2b) was introduced that avoids lead azide as a hazardous byproduct.
Abstract: 1,5-Diamino-1H-tetrazole (2, DAT) can easily be protonated by reaction with strong mineral acids, yielding the poorly investigated 1,5-diaminotetrazolium nitrate (2a) and perchlorate (2b). A new synthesis for 2 is introduced that avoids lead azide as a hazardous byproduct. The reaction of 1,5-diamino-1H-tetrazole with iodomethane (7a) followed by the metathesis of the iodide (7a) with silver nitrate (7b), silver dinitramide (7c), or silver azide (7d) leads to a new family of heterocyclic-based salts. In all cases, stable salts were obtained and fully characterized by vibrational (IR, Raman) spectroscopy, multinuclear NMR spectroscopy, mass spectrometry, elemental analysis, X-ray structure determination, and initial safety testing (impact and friction sensitivity). Most of the salts exhibit good thermal stabilities, and both the perchlorate (2b) and the dinitramide (7c) have melting points well below 100 degrees C, yet high decomposition onsets, defining them as new (7c), highly energetic ionic liquids. Preliminary sensitivity testing of the crystalline compounds indicates rather low impact sensitivities for all compounds, the highest being that of the perchlorate (2b) and the dinitramide (7c) with a value of 7 J. In contrast, the friction sensitivities of the perchlorate (2b, 60 N) and the dinitramide (7c, 24 N) are relatively high. The enthalpies of combustion (Delta(c)H degrees ) of 7b-d were determined experimentally using oxygen bomb calorimetry: Delta(c)H degrees (7b) = -2456 cal g(-)(1), Delta(c)H degrees (7c) = -2135 cal g(-)(1), and Delta(c)H degrees (7d) = -3594 cal g(-)(1). The standard enthalpies of formation (Delta(f)H degrees ) of 7b-d were obtained on the basis of quantum chemical computations using the G2 (G3) method: Delta(f)H degrees (7b) = 41.7 (41.2) kcal mol(-)(1), Delta(f)H degrees (7c) = 92.1 (91.1) kcal mol(-)(1), and Delta(f)H degrees (7d) = 161.6 (161.5) kcal mol(-)(1). The detonation velocities (D) and detonation pressures (P) of 2b and 7b-d were calculated using the empirical equations of Kamlet and Jacobs: D(2b) = 8383 m s(-)(1), P(2b) = 32.2 GPa; D(7b) = 7682 m s(-)(1), P(7b) = 23.4 GPa; D(7c) = 8827 m s(-)(1), P(7c) = 33.6 GPa; and D(7d) = 7405 m s(-)(1), P(7d) = 20.8 GPa. For all compounds, a structure determination by single-crystal X-ray diffraction was performed. 2a and 2b crystallize in the monoclinic space groups C2/c and P2(1)/n, respectively. The salts of 7 crystallize in the orthorhombic space groups Pna2(1) (7a, 7d) and Fdd2 (7b). The hydrogen-bonded ring motifs are discussed in the formalism of graph-set analysis of hydrogen-bond patterns and compared in the case of 2a, 2b, and 7b.

229 citations

Journal ArticleDOI
TL;DR: The disilyne R**Si≡SiR** (R** = SiMe(SitBu3)2) was prepared as the first isolable and realtively stable silicon compound with a SiSi triple bond two years ago by dehalogenation of trans-R**ClSi=SiClR** with LiC10H8 in thf at -78 °C (calc: Si≡si distance 2.072A, Si-Si>Si bond angle 148°), forms with CH2=CH2 a [2+2]
Abstract: The disilyne R**Si≡SiR** (R** = SiMe(SitBu3)2), prepared as the first isolable and realtively stable silicon compound with a SiSi triple bond two years ago by dehalogenation of trans-R**ClSi=SiClR** with LiC10H8 in thf at -78 °C (calc.: Si≡Si distance 2.072A, Si-Si≡Si bond angle 148°), forms with CH2=CH2 a [2+2] and with CH2=CH-CH=CH2 a [2+4] cycloadduct. The ethene adduct takes up oxygen very easily with change of the Si=Si group into a SiOSiO ring with formation of R**Si(μ-O)(μ-O)(μ-C2H4)SiR**. By heating the disilyne in heptane to ca. 50 °C in the presence of traces of thf it transforms into a monoxide of the ethene adduct with formation of R**Si(μ-O)(μ-C2H4)SiR**. In thf, the disilyne rearranges at r.t. and below by migration of a SitBu3 group with formation of a silyl substituted cyclotrisilene. X-ray structure determinations of the ethene adduct and its mono- and dioxide are presented.

212 citations

Journal ArticleDOI
TL;DR: The highly friction-sensitive 1,5-diamino-4-methyltetrazolium dinitramide was synthesized by a metathetical reaction of the corresponding iodide and silver dinitramside, and the chemical bond is discussed on the basis of the theory of atoms in molecules (AIM).
Abstract: The highly friction-sensitive 1,5-diamino-4-methyltetrazolium dinitramide was synthesized by a metathetical reaction of the corresponding iodide and silver dinitramide. An intriguing interaction of one nitro group with the tetrazolium cation was found as a crystal structure determining feature (X-ray determination), and the chemical bond is discussed on the basis of the theory of atoms in molecules (AIM).

194 citations

Journal ArticleDOI
TL;DR: The α−β phase transition in 1,1-diamino-2,2-dinitroethylene, C2H4N4O4 (FOX-7) has been studied by single-crystal X-ray investigations at five different temperatures in this article.
Abstract: The α−β phase transition in the novel energetic material 1,1-diamino-2,2-dinitroethylene, C2H4N4O4 (FOX-7), has been studied by single-crystal X-ray investigations at five different temperatures ov...

187 citations


Cited by
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28 Jul 2005
TL;DR: PfPMP1)与感染红细胞、树突状组胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作�ly.
Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1(PfPMP1)与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员,通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

18,940 citations

Journal ArticleDOI
01 Apr 1988-Nature
TL;DR: In this paper, a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) is presented.
Abstract: Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

9,929 citations

Journal ArticleDOI
10 Mar 1970

8,159 citations

Journal ArticleDOI
TL;DR: The current knowledge in the structure and chemistry of cellulose, and in the development of innovative cellulose esters and ethers for coatings, films, membranes, building materials, drilling techniques, pharmaceuticals, and foodstuffs are assembled.
Abstract: As the most important skeletal component in plants, the polysaccharide cellulose is an almost inexhaustible polymeric raw material with fascinating structure and properties. Formed by the repeated connection of D-glucose building blocks, the highly functionalized, linear stiff-chain homopolymer is characterized by its hydrophilicity, chirality, biodegradability, broad chemical modifying capacity, and its formation of versatile semicrystalline fiber morphologies. In view of the considerable increase in interdisciplinary cellulose research and product development over the past decade worldwide, this paper assembles the current knowledge in the structure and chemistry of cellulose, and in the development of innovative cellulose esters and ethers for coatings, films, membranes, building materials, drilling techniques, pharmaceuticals, and foodstuffs. New frontiers, including environmentally friendly cellulose fiber technologies, bacterial cellulose biomaterials, and in-vitro syntheses of cellulose are highlighted together with future aims, strategies, and perspectives of cellulose research and its applications.

6,098 citations

Journal ArticleDOI
TL;DR: This review covers the literature published in 2014 for marine natural products, with 1116 citations referring to compounds isolated from marine microorganisms and phytoplankton, green, brown and red algae, sponges, cnidarians, bryozoans, molluscs, tunicates, echinoderms, mangroves and other intertidal plants and microorganisms.

4,649 citations