ChemInform Abstract: CYCLOPROPYLIDENEMETHANONE: A QUASI-SYMMETRICAL MOLECULE

1985 ◽  
Vol 16 (15) ◽  
Author(s):  
R. D. BROWN ◽  
P. D. GODFREY ◽  
B. KLEIBOEMER ◽  
R. CHAMPION ◽  
P. S. ELMES
Keyword(s):  
1984 ◽  
Vol 106 (25) ◽  
pp. 7715-7718 ◽  
Author(s):  
Ronald D. Brown ◽  
Peter D. Godfrey ◽  
Burkhard Kleiboemer ◽  
Robert Champion ◽  
Patricia S. Elmes
Keyword(s):  

1968 ◽  
Vol 23 (2) ◽  
pp. 259-268 ◽  
Author(s):  
E. Leistner ◽  
M. H. Zenk

The biosynthesis of 5-hydroxy-1,4-naphthoquinone (juglone) was studied by supplying radioactive precursors to leaves of Juglans regia plants. A chemical degradation of the juglone molecule was devised (Fig. 1). With these methods it was shown that the ring atoms of shikimic acid are incorporated into the benzene ring of the quinone, while the carboxyl group of this acid is transformed to 50% into each of the keto groups of the quinone ring (C-atoms 1 and 4 of juglone. Tab. 3). This suggested a symmetrical molecule to be an intermediate in the formation of juglone — most probable 1,4-naphthoquinone. This compound was synthetized with 14C in the positions 2, 3, 9, and 10 and was found to be a good precursor of juglone in Juglans as well as for 2-hydroxy-1,4-naphthoquinone in Impatiens plants (Tab. 4) . 3,4-Dihydroxybenzaldehyde (Tab. 2) and chorismic acid (Tab. 7) which have been suggested previously as intermediates in the biosynthesis of naphthoquinones are no precursors of juglone. The source of three carbon atoms of the quinone nucleus remains to be determined; one or two of these carbon atoms (C2 and/or C3 of juglone) are formed from the methylen carbon of malonate (Tab. 5 and 6); surprisingly, however, the carboxyl carbons of malonic acid are not incorporated. The substitution of shikimic acid occures in the position 6 of this acid as could be judged from the degradation of juglone labelled with shikimic acid [ 1,2-14C] (Fig. 2; Tab. 3). 1,4-Naphthoquinone (or naphthohydroquinone) is postulated as an important intermediate in the biosynthesis of naphthoquinone derivatives in higher plants.


It has now been known for several years that the molecules of a gas consisting of positive and negative charges set into forced vibrations by the electric field of an incident light-wave are responsible, not only for the refractive properties of the medium, but also for lateral scattering and extinction as exemplified on a large scale by the blue of the sky and the colour of the setting sun. In fact, until comparatively recently, observations on the extinction of solar radiation of various wave-lengths by the earth’s atmosphere have provided the only dataf by means of which the theory of molecular scattering and extinction could be tested, this by satisfactory evaluations of the number of molecules per cubic centimetre of air under standard conditions of temperature and pressure, making use for the purpose of Rayleigh’s well-known extinction formula based on the idea of the symmetrical molecule , i.e. , one in which the dispersion electrons move in the direction of the electric vector in the lightwavewave. As far as observations were then available, theory gave a tolerably good account of measurements of sky-intensity, both as regards quality and polarization. The difficulty in this case is to take into account the illumination of the atmosphere by itself, a problem capable of reasonably simple solution in terms of integral equations only if the curvature of the earth is disregarded. From the experimental point of view, satisfactory observations are made difficult by the omnipresent and ever-varying dust content of the atmosphere at ordinary levels, to say nothing of the “ haziness ” and extinction due to the presence of water-vapour.


2008 ◽  
Vol 607 ◽  
pp. 25-29 ◽  
Author(s):  
David M. Schrader

Dipositronium, Ps2, was recently prepared [1]. This is significant because: • It is the first laboratory observation of a molecule that contains more than one positron; • It is the most symmetrical molecule possible; • It is the most non-rigid (floppiest) molecule possible; • The interval between the theoretical establishment of its existence [2] and its laboratory observation [1] is inordinately long – 60 years; and • An extension of the technology developed for the Ps2 observation may soon lead to an observation of the Bose-Einstein condensation of positronium and the development of a gamma ray laser. We briefly discuss the symmetry of Ps2 and how an understanding of it will underlie its characterization in the future. Ps2O and CPs2 might be the next two-positron compounds to be prepared and characterized in the laboratory. A discussion of the contrasting eigenstates of these two molecules is given. An understanding of these states is required in order to identify them.


IUCrData ◽  
2018 ◽  
Vol 3 (7) ◽  
Author(s):  
Marvin J. Böhm ◽  
Christopher Golz ◽  
Manuel Alcarazo

The C 3-symmetrical molecule, tris(4-methoxyphenyl)stibine, C21H21O3Sb, crystallizes with one third of the molecule in the asymmetric unit. Bond lengths and angles of the Sb—C bonds lie in between those of the isostructural homologues C21H21O3Bi and C21H21O3As. The formation of dimers via six weak C—H...π interactions is considered.


1998 ◽  
Vol 142 (6) ◽  
pp. 1595-1604 ◽  
Author(s):  
Thomas E. Melby ◽  
Charles N. Ciampaglio ◽  
Gina Briscoe ◽  
Harold P. Erickson

Structural maintenance of chromosomes (SMC) proteins function in chromosome condensation and several other aspects of DNA processing. They are large proteins characterized by an NH2-terminal nucleotide triphosphate (NTP)-binding domain, two long segments of coiled coil separated by a hinge, and a COOH-terminal domain. Here, we have visualized by EM the SMC protein from Bacillus subtilis (BsSMC) and MukB from Escherichia coli, which we argue is a divergent SMC protein. Both BsSMC and MukB show two thin rods with globular domains at the ends emerging from the hinge. The hinge appears to be quite flexible: the arms can open up to 180°, separating the terminal domains by 100 nm, or close to near 0°, bringing the terminal globular domains together. A surprising observation is that the ∼300–amino acid–long coiled coils are in an antiparallel arrangement. Known coiled coils are almost all parallel, and the longest antiparallel coiled coils known previously are 35–45 amino acids long. This antiparallel arrangement produces a symmetrical molecule with both an NH2- and a COOH-terminal domain at each end. The SMC molecule therefore has two complete and identical functional domains at the ends of the long arms. The bifunctional symmetry and a possible scissoring action at the hinge should provide unique biomechanical properties to the SMC proteins.


1983 ◽  
Vol 0 (22) ◽  
pp. 1289-1290 ◽  
Author(s):  
Thomas M. Marschner ◽  
Mark A. Reynolds ◽  
Norman J. Oppenheimer ◽  
George L. Kenyon

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