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M Marangoni

Publications and source records attributed to M Marangoni.

10 recordsLinked to original sources
PubMed2006

Simultaneously phase-matched second- and third-harmonic generation from 1.55 microm radiation in annealed proton-exchanged periodically poled lithium niobate waveguides.

Third-harmonic generation (THG) in the cw regime from C-band radiation was achieved in annealed proton-exchanged periodically poled lithium niobate (PPLN) waveguides. By suitable design of fabrication parameters and operating conditions, quasi-phase-matching (QPM) is obtained simultaneously for the second-harmonic generation process (omega-->2omega, first-order QPM) and for the sum-frequency-generation process (omega+2omega-->3omega, third-order QPM), which provides the third harmonic of the pump field. The high overlap between the field profiles of the interacting modes--TM00 at omega and TM10 at 2omega and 3omega--results in what is believed to be the highest ever reported normalized conversion efficiency for THG from telecommunication wavelengths, equal to 0.72%W(-2) cm(-4).

Journal Article↗
PubMed2006

Observation of dynamic localization in periodically curved waveguide arrays.

We report on a direct experimental observation of dynamic localization (DL) of light in sinusoidally-curved lithium-niobate waveguide arrays which provides the optical analog of DL for electrons in periodic potentials subjected to ac electric fields as originally proposed by Dunlap and Kenkre [Phys. Rev. B 34, 3625 (1986)10.1103/PhysRevB.34.3625]. The theoretical condition for DL in a sinusoidal field is experimentally demonstrated.

Journal Article↗
PubMed2006

Optical-damage-free guided second-harmonic generation in 1% MgO-doped stoichiometric lithium tantalate.

Room-temperature cw second-harmonic generation from telecom wavelengths, with 30% W(-1) cm(-2) efficiency and second-harmonic power levels up to 41 mW, was achieved in buried waveguides fabricated by reverse-proton exchange in 1% MgO-doped stoichiometric lithium tantalate without any evidence of optical damage. The technology proves suitable for the realization of efficient nonlinear frequency converters and all-optical devices.

Journal Article↗
PubMed2005

Beam dynamics and wave packet splitting in a periodically curved optical waveguide: multimode effects.

A theoretical and experimental analysis of beam dynamics and wave packet splitting of light in a periodically bent optical waveguide, a phenomenon recently observed [Phys. Rev. Lett. 94, 073002 (2005)] which is the optical equivalent of adiabatic stabilization of atoms in intense and high-frequency laser fields, is presented in the multimode operational regime. Inhibition of wave packet splitting is theoretically predicted and experimentally observed for higher-order mode excitation.

Journal Article↗
PubMed1997

Synthesis and hybridization properties of inverse oligonucleotides.

The synthesis of adenine and thymine cyclopentylethyl nucleosides is presented. This novel constrained monomeric building block is very difficult to incorporate into oligonucleotides. It was introduced in 13mer oligodeoxynucleotide sequences at a single position using H-phosphonate chemistry. Phosphoramidite chemistry completely failed in this particular case. The H-phosphonate building blocks were obtained starting from the corresponding phosphoramidites. Stability of duplexes with RNA and DNA is significantly reduced.

Chromosome Inversion↗
PubMed1996

Pyrazole-related nucleosides. 4. Synthesis and antitumor activity of some 1-tetrahydropyranyl-4-substituted pyrazoles.

Continuing our studies on the structure-activity relationships of some pyrazole nucleosides (1a-h) structurally related to ribavirin, tiazofurin and selenazofurin, we describe here the synthesis and antitumor/antiviral/antimicrobial activity of a new series of 1-tetrahydropyranyl-4-substituted pyrazoles. In this study, the tetrahydropyranyl moiety (THP), designed as a mimic of the glycosidic portion of the parent compounds 1a-h, has led to a few derivatives with moderate cytotoxic activity against leukemia/lymphoma and solid tumor-derived cell lines (IC50 14-100 microM). The compounds obtained through substitution of the ribofuranosyl moiety by the THP moiety were still active, the free heterocyclic bases were devoid of any activity.

Animals↗
PubMed1995

Synthesis and cytotoxic activity of 6-vinyl- and 6-ethynyluridine and 8-vinyl-and 8-ethynyladenosine.

It is well-known that the introduction of vinyl and ethynyl moieties into nucleosides is of crucial importance for cytostatic, antiviral, or other biological activities. In this study 6- and 8-vinyl-and -ethynyluridine and -adenosine were prepared by a general procedure involving the palladium-catalyzed cross-coupling of trimethylsilylacetylene or vinyltributyltin. The introduction of a vinyl group at C-6 of uridine or an ethynyl group at C-8 of adenosine resulted in nucleoside derivatives showing cytostatic activity against several murine and/or human tumor cell lines. Interestingly, 8-vinyladenosine had pronounced selective inhibitory effects on human (Molt/4F and MT-4) versus murine (L1210 and FM3A) tumor cell lines.

Adenosine↗
PubMed1988

Coincidence 16O(e

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Journal Article↗