Positive working photoresists sensitive to visible light,II: poly{2-arylpropyl-2 and bis(p-methoxyphenyl)methyl methacrylates}

Acid-labile polymers of methacrylates of 2-(p-substituted phenyl)propanol-2 and bis(p-methoxyphenyl)methanol were evaluated as visible light sensitive positive-type resists. The chemistry to form images is based on the cleavage of esters catalysed by an acid generated by photodecomposition of diphenyliodonium hexafluorophosphate sensitized by 2-benzoyl-3-(p-dimethylaminophenyl)-2-propenenitrile. A copolymer of bis(p-methoxyphenyl)methyl methacrylate-phenyl methacrylate exhibited a high photospeed upon exposure to 488 nm light when coupled with the iodonium salt and the dye, and was applicable to relief holography.     

Canonical formulation of magnetic domain-wall motion

We revisit a long-standing problem concerning the inertial mass of a magnetic domain wall (DW) motion. Using constrained Hamiltonian formalism, we set up the macroscopic physical Hamiltonian describing the free-particle-like motion of the DW starting with the micromagnetic Lagrangian density.     

Doyle-Kirmse reaction of allylic sulfides with diazoalkane-free (2-furyl)carbenoid transfer

[reaction: see text] In the presence of rhodium catalyst, (2-furyl)carbenoids generated from conjugated ene-yne-carbonyl compounds 1 efficiently undergo carbene transfer reactions with allylic sulfides followed by [2,3]sigmatropic rearrangement of sulfur ylides to give furan-containing sulfides in good yields. When diallyl sulfide is employed, heteroatom-containing polycyclic compounds are obtained by sequential intramolecular Diels-Alder cyclization reaction with a constructed furan ring as an enophile.     

Synthesis of Vinylene-Co,N-Linked Multi(porphyrin)s by the Addition of Free-Base Porphyrins to a C(2)H(2) Complex of Cobalt(III) Porphyrin and Their Oxidative Rearrangement to Vinylene-N,N'-Linked Multi(porphyrin)s

The nucleophilic addition reaction of a pyrrole nitrogen of free-base porphyrins to a pi-complexed acetylene ligand in a cationic Co(III) porphyrin intermediate afforded good yields of vinylene-Co,N'-linked bis(porphyrin)s, (Por)Co(III)-CH=CH-(N-Por)H(2). N-substituted porphyrin free bases are N-vinylated regioselectively at the pyrrole adjacent to the original N-substituted pyrrole in this reaction. Tris- and tetrakis(porphyrin)s have been prepared by reacting a vinylene-N,N'-linked bis(meso-tetraarylporphyrin) with (OEP)Co(III)(H(2)O)(2)ClO(4) (OEP: octaethylporphyrin dianion) and acetylene. The tetrakis(porphyrin) proved to be a 1:1 mixture of C(i)()- and C(2)-symmetric regioisomers. These organometallic Co(III) complexes underwent facile oxidative migration of the Co-bound vinyl group to a porphyrin pyrrole nitrogen when treated with Fe(III) salts or HClO(4) to provide moderate to good yields of Co(II) vinylene-N,N'-linked multi(porphyrin) complexes. (Vinylene-N,N')bis(porphyrin) free bases with combinations of different porphyrins have been obtained by this procedure. The homobinuclear (2Co(II), 2Cu(II), and 2Zn(II)) and heterobinuclear (Co(II)Cu(II) and Co(II)Zn(II)) complexes have been prepared and characterized spectroscopically. The single-crystal X-ray analysis of (CH=CH-N,N')[(OEP)Co(II)Cl][(TPP)Zn(II)Cl] (TPP: meso-tetraphenylporphyrin dianion) showed a face-to-face structure with an average inter-ring separation of 4.39 ? (triclinic P&onemacr;; Z = 2; a = 14.806(4), b = 18.703(10), c = 13.796(3) ?, alpha = 97.69(3), beta = 99.57(2), gamma = 96.74(3) degrees ).     

Spin and orbital excitations in perovskite Mn oxides

An effective Hamiltonian of perovskite type LaMnO₃ is derived by taking into account the degeneracy ofe _g orbitals, Hund coupling and strong Coulomb interactions betweend-electrons in Mn ions. Spin and orbital excitations are calculated by using the effective Hamiltonian.