✦ LIBER ✦

The radion in 5D conformal SUGRA: superspace action

✍ Scribed by F. Paccetti Correia; M.G. Schmidt; Z. Tavartkiladze

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 115 KB
Volume: 53
Category: Article
ISSN: 0015-8208
DOI: 10.1002/prop.200510224

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

We shortly review our new superfield formalism in the framework of Fujita, Kugo, Ohashi 5D conformal supergravity, in particular with an S^1^/Z~2~ orbifold. The radion of the fifth dimension is embedded in two related superfields, a chiral and a general multiplet and is linked to the radion superfield of rigid SUSY. The superspace action of the gauge sector is of the Chern‐Simons type. We also present the superspace action for hypermultiplets and discuss the role of compensators. The presented formalism should be very useful for applications. We demonstrate this for obtaining the RS solution.

📜 SIMILAR VOLUMES

The occurrence, conformation and crystal

The occurrence, conformation and crystal structure of 1,5-anhydro-d-glucitol in Protea spp.

✍ J.C.A. Boeyens; J.L.C. Marais; G.W. Perold 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 195 KB

Amino acid residues involved in the acti

Amino acid residues involved in the action of endo-(1→3)-β-d-glucanase II from Flavobacterium dormitator var. glucanolyticae FA-5

✍ Shinpei Yamamoto; Masamitsu Miyagi; Susumu Nagasaki 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 536 KB

The pa-dependence of the kinetic parameters for the hydrolysis of yeast glucan with endo-(1 +3)-fl-~glucanase II from Flav. dormitator var. glucanolyticae FA-5 suggests that two residues (histidyl and carboxyl) are involved in the enzyme action. Chemical modification of the enzyme has been studied i

Configuration-dependent conformational t

Configuration-dependent conformational transmission in trigonal-bipyramidal Pv compounds. Enhanced gauche (-) population around the C(5)-C(6) linkage in 6-Pv phosphorylated tetramethyl-α-D-galactopyranoside

✍ N. K. de Vries; H. M. Buck 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 632 KB

X-ray crystal structures of 1,2,4-tri-O-

X-ray crystal structures of 1,2,4-tri-O-acetyl-5-deoxy-3-O-methyl-5-[(S)-phenylphosphinyl]-α-d-xylopyranose and its 5-[(S-phenylphosphinothioyl] derivative, and conformations of d-xylopyranose analogs having a C6H5P(R) group in the hemiacetal ring

✍ Thomas Richter; Peter Luger; Tadashi Hanaya; Hiroshi Yamamoto 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 780 KB

X-ray crystallographic analyses are reported for the two title compounds (8 and 9), of which the former crystallized in two modifications (8n and 8b). In all three structures, the pyranose rings have the %, (D) conformation and the substituents at C-l are axial and those at C-24-4 are equatorial. Th

Nucleic Acid Analogs with Constraint Con

Nucleic Acid Analogs with Constraint Conformational Flexibility in the Sugar-Phosphate Backbone “Tricyclo-DNA”. Part 1. Preparation of [(5′R,6′R)-2′-deoxy-3′,5′-ethano-5′,6′-methano-β-D-ribofuranosyl]thymine and -adenine, and the corresponding phosphoramidites for oligonucleotide synthesis

✍ Ralph Steffans; Christian Leumann 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 German ⚖ 1019 KB

In extension of the bicyclo-DNA nomenclature (see , Foornote 3), the name tricyclo-DNA and, correspondingly, tricyclo-deoxynucleosides was chosen to denominate this type of nucleotide and nucleoside analog. ## The numbering scheme as depicted in Fig. f for nucleosides was chosen in order to be ab

ChemInform Abstract: Nucleic-Acid Analog

ChemInform Abstract: Nucleic-Acid Analogues with Constraint Conformational Flexibility in the Sugar—Phosphate Backbone ′Tricyclo-DNA′. Part 1. Preparation of [(5′R,6′R)-2′-Deoxy-3′,5′-ethano-5′,6′-methano-β-D-ribofuranosyl] thymine and -adenine, and the Corresponding Phosphoramidites for Oligonucleotide Synthesis.

✍ R. STEFFENS; C. LEUMANN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Nucleic-Acid Analogues with Constraint Conformational Flexibility in the Sugar-Phosphate Backbone 'Tricyclo-DNA'. Part 1. Preparation of [(5'R,6'R)-2'-Deoxy-3',5'-ethano-5',6'-methano-β-D-ribofuranosyl] thymine and -adenine, and the Corresponding Phosphoramidites for Oligonucleotide Synthesis. -An