Demchuk, Oleg M.’s team published research in Tetrahedron in 72 | CAS: 2960-93-2

Tetrahedron published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Category: naphthyridine.

Demchuk, Oleg M. published the artcileReadily available catalysts for demanding Suzuki-Miyaura couplings under mild conditions, Category: naphthyridine, the publication is Tetrahedron (2016), 72(42), 6668-6677, database is CAplus.

A straightforward synthesis of a sterically hindered and electron rich bidentate monophosphine biaryl ligand Sym-Phos (I) exhibiting C,P-type of complexation was realized in a high yield starting from simple substrates in easily affordable conditions. In combination with a palladium source, the obtained ligand formed a highly active catalyst mediating sterically demanding Suzuki-Miyaura coupling reactions in aqueous media even at 60 °C and with no need to protect the reaction mixture by an inert gas.

Tetrahedron published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Category: naphthyridine.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Masuya, Yoshihiro’s team published research in Synlett in 30 | CAS: 2960-93-2

Synlett published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Category: naphthyridine.

Masuya, Yoshihiro published the artcileThiolate-Initiated Synthesis of Dibenzothiophenes from 2,2′-Bis(methylthio)-1,1′-Biaryl Derivatives through Cleavage of Two Carbon-Sulfur Bonds, Category: naphthyridine, the publication is Synlett (2019), 30(17), 1995-1999, database is CAplus.

Thiolate-initiated synthesis of dibenzothiophenes from 2,2′-bis(methylthio)-1,1′-biaryl derivatives through cleavage of two carbon-sulfur bonds was developed. This reaction did not require a transition-metal catalyst and was promoted by a thiolate anion. Notably, based on DFT calculations, the product-forming cyclization step was shown to proceed through a concerted nucleophilic aromatic substitution (CSNAr) mechanism. Furthermore, this metathesis protocol enabled the method to be expanded to double carbon-oxygen bonds and carbon-oxygen/carbon-sulfur metathesis.

Synlett published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Category: naphthyridine.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Briza, Tomas’s team published research in Organic Letters in 7 | CAS: 2960-93-2

Organic Letters published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Application of 2,2′-Dimethoxy-1,1′-binaphthalene.

Briza, Tomas published the artcileChromophoric Binaphthyl Derivatives, Application of 2,2′-Dimethoxy-1,1′-binaphthalene, the publication is Organic Letters (2005), 7(17), 3661-3664, database is CAplus and MEDLINE.

A short synthetic route is outlined, starting from bromobinaphthyl derivatives, via halogen lithium exchange, subsequent Michael reaction with dimethylaminoacrolein, hydrolysis to the corresponding aldehyde, and final condensation with a benzothiazolium unit to produce a binaphthyl-pentamethinium system, which absorbs in the visible range around 450 nm. Enantiopure ligands show a good Cotton effect in the CD spectrum. Preliminary data show potential of these compounds in the area of supramol. chem. (enantioselective recognition) and also for medicinal application (induction of apoptosis).

Organic Letters published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Application of 2,2′-Dimethoxy-1,1′-binaphthalene.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Demchuk, Oleg M.’s team published research in Pure and Applied Chemistry in 83 | CAS: 2960-93-2

Pure and Applied Chemistry published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Formula: C22H18O2.

Demchuk, Oleg M. published the artcileRational design of novel ligands for environmentally benign cross-coupling reactions, Formula: C22H18O2, the publication is Pure and Applied Chemistry (2011), 83(3), 633-644, database is CAplus.

Transition-metal (TM) complexes of new phosphines, readily prepared by a straightforward three-step modular synthesis, were successfully employed in difficult cross-coupling reactions conducted under mild conditions (water, “open-flask”, low temperature) that aspire to meet green chem. criteria. High yielding catalyzed by bismuth or rhodium complexes oxidative arylation of naphthoquinone gave the key 2-aryl naphthoquinone intermediates for facile bismuth triflate-catalyzed Michael addition of secondary phosphine oxides. Subsequent O-methylation and reductions of the resulting products gave access to the target air-stable phosphine ligands in good overall yields (up to 60%).

Pure and Applied Chemistry published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Formula: C22H18O2.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Ma, Qiang’s team published research in Polymer Chemistry in 13 | CAS: 2960-93-2

Polymer Chemistry published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene.

Ma, Qiang published the artcileOrganocatalytic orthogonal ATRP and ring-opening polymerization using a single dual-function photocatalyst, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene, the publication is Polymer Chemistry (2022), 13(29), 4284-4289, database is CAplus.

Orthogonal catalysis is emerging as a powerful method for the synthesis of block copolymers. By employing a single designed dual-function photoredox phosphoric acid catalyst (Photo-PA), two types of polymerizations via different mechanisms, photo-triggered organocatalyzed atom transfer radical polymerization and acid-triggered ring-opening polymerization, can be effectively bridged, discriminated and performed simultaneously in one pot. This orthogonal system also features metal-free conditions, visible light regulation, the use of a single catalyst, as well as good compatibility and control, allowing the synthesis of block copolymers with the desired component and low dispersity in a one-pot approach and controlled manner.

Polymer Chemistry published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Zhang, Linlin’s team published research in Chemical Engineering Journal (Amsterdam, Netherlands) in 426 | CAS: 159-62-6

Chemical Engineering Journal (Amsterdam, Netherlands) published new progress about 159-62-6. 159-62-6 belongs to naphthyridine, auxiliary class Other Aromatic Heterocyclic,Spiro, name is Spiro[fluorene-9,9′-xanthene], and the molecular formula is C11H12O4, Quality Control of 159-62-6.

Zhang, Linlin published the artcileCross-conjugated spiro molecules and single-walled carbon nanotubes composite for high-performance organic thermoelectric materials and generators, Quality Control of 159-62-6, the publication is Chemical Engineering Journal (Amsterdam, Netherlands) (2021), 131859, database is CAplus.

Organic thermoelec. materials have attracted tremendous attention in virtue of their unique advantages including low thermal conductivity, low cost, easy processability and mech. flexibility. Herein, a series of novel Spiro mols. are designed to be composited with single-walled carbon nanotubes (SWCNT) as p-type thermoelec. materials. An optimum power factor of 218.6μW m-1 K-2 is acquired from the SFX-2/SWCNT composite at room temperature The corresponding flexible thermoelec. generator containing 10p-type legs exhibits an output power of 1.0μW under a temperature gradient of 60 K. The high thermoelec. performance is attributable to the three dimensional cross-conjugated architecture of the Spiro mols., which promotes interactions with SWCNT leading to high carrier concentration and moderate carrier mobility in the composite film.

Chemical Engineering Journal (Amsterdam, Netherlands) published new progress about 159-62-6. 159-62-6 belongs to naphthyridine, auxiliary class Other Aromatic Heterocyclic,Spiro, name is Spiro[fluorene-9,9′-xanthene], and the molecular formula is C11H12O4, Quality Control of 159-62-6.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Gribkov, Denis V.’s team published research in Chemistry – A European Journal in 9 | CAS: 2960-93-2

Chemistry – A European Journal published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Name: 2,2′-Dimethoxy-1,1′-binaphthalene.

Gribkov, Denis V. published the artcileSynthesis and characterization of new biphenolate and binaphtholate rare-earth-metal amido complexes: Catalysts for asymmetric olefin hydroamination/cyclization, Name: 2,2′-Dimethoxy-1,1′-binaphthalene, the publication is Chemistry – A European Journal (2003), 9(19), 4796-4810, database is CAplus and MEDLINE.

Monomeric diolate amido yttrium complexes [Y{diolate}{N(SiHMe2)2}(THF)2] can be prepared in good yield by treating [Y{N(SiHMe2)2}3(THF)2] with either 3,3′-di-tert-butyl-5,5′,6,6′-tetramethyl-1,1′-biphenyl-2,2′-diol (H2(Biphen)), 3,3′-bis(2,4,6-triisopropylphenyl)-2,2′-dihydroxy-1,1′-dinaphthyl (H2(Trip2BINO)) or 3,3′-bis(2,6-diisopropylphenyl)-2,2′-dihydroxy-1,1′-dinaphthyl (H2(Trip2BINO)) in racemic and enantiopure form. The racemic complex [Y(biphen){N(SiHMe2)2}(THF)2] dimerizes upon heating to give the heterochiral complex (R,S)-[Y(biphen){N(SiHMe2)2}(THF)]2. The corresponding dimeric heterochiral lanthanum complex was the sole product in the reaction of H2(Biphen) with [La{N(SiHMe2)2}3(THF)2]. Single-crystal x-ray diffraction of both dimeric complexes revealed that the two Ln(biphen){N(SiHMe2)2}(THF) fragments are connected through bridging phenolate groups of the biphenolate ligands. The two different phenolate groups undergo an intramol. exchange process in solution leading to their equivalence on the NMR timescale. All complexes were active catalysts for the hydroamination/cyclization of aminoalkynes and aminoalkenes at elevated temperature, with [Y((R)-dip2bino){N(SiHMe2)2}(THF)2] being the most active one giving enantioselectivities of up to 57% ee. Kinetic resolution of 2-aminohex-5-ene proceeded with this catalyst with 6.4:1 trans selectivity to give 2,5-dimethylpyrrolidine with a krel of 2.6.

Chemistry – A European Journal published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Name: 2,2′-Dimethoxy-1,1′-binaphthalene.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Morioka, Kohei’s team published research in Polymer Journal (Tokyo, Japan) in 37 | CAS: 2960-93-2

Polymer Journal (Tokyo, Japan) published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene.

Morioka, Kohei published the artcileSynthesis, chiroptical properties, and chiral recognition ability of optically active polymethacrylamides having various tacticities, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene, the publication is Polymer Journal (Tokyo, Japan) (2005), 37(4), 299-308, database is CAplus.

The radical polymerization of optically active methacrylamides, such as N-[(R)-(+)-α-methylbenzyl]methacrylamide, N-[(R)-(-)-1-cyclohexylethyl]methacrylamide, N-[(R)-(+)-1-(1-naphthyl)ethyl]methacrylamide, and N-[(1R,2S)-(-)-1-(2-indanol)methacrylamide, was carried out under various conditions. The polymerization in the presence of ytterbium trifluoromethanesulfonate [Yb(OTf)3] produced isotactic-rich polymers compared with those obtained without the Lewis acid. The sp. rotations and the CD spectral patterns of the obtained polymers varied with the tacticities, suggesting that the tacticities influence the secondary structures of the polymers. The IR spectra of the polymers indicated that the isotactic polymers favorably formed intramol. hydrogen bonds. The chiral recognition ability of the optically active polymers immobilized on silica gel was evaluated as the chiral stationary phases for high-performance liquid chromatog. (HPLC).

Polymer Journal (Tokyo, Japan) published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Safety of 2,2′-Dimethoxy-1,1′-binaphthalene.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Maciejczyk, Michal’s team published research in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 4 | CAS: 159-62-6

Journal of Materials Chemistry A: Materials for Energy and Sustainability published new progress about 159-62-6. 159-62-6 belongs to naphthyridine, auxiliary class Other Aromatic Heterocyclic,Spiro, name is Spiro[fluorene-9,9′-xanthene], and the molecular formula is C25H16O, SDS of cas: 159-62-6.

Maciejczyk, Michal published the artcileSFX as a low-cost ‘Spiro’ hole-transport material for efficient perovskite solar cells, SDS of cas: 159-62-6, the publication is Journal of Materials Chemistry A: Materials for Energy and Sustainability (2016), 4(13), 4855-4863, database is CAplus.

Four spiro[fluorene-9,9′-xanthene] (SFX) derivatives, SFX-TAD, SFX-TCz, SFX-TPTZ and SFX-MeOTAD have been synthesized for use as hole-transport materials and fully characterized by 1H/13C NMR spectroscopy, mass spectrometry, XRD and DSC. Their thermal, optical and electrochem. properties were investigated. The use of different substituents affects the HOMO (HOMO) energy level proving the versatility of the central core towards the facile and low-cost preparation of spiro-hole-transport materials. Among the synthesized SFX derivatives, SFX-MeOTAD was employed as hole-transporting material (HTM) and the performance tested in perovskite solar cells with device architecture glass/FTO/compact TiO2/mesoporous Al2O3/CH3NH3PbI3-xClx/HTM/Au. SFX-MeOTAD gave a comparable efficiency to spiro-MeOTAD, demonstrating great potential for use of the SFX family as cost effective and versatile hole conductors facilitating commercialization of perovskite solar cells (PSCs).

Journal of Materials Chemistry A: Materials for Energy and Sustainability published new progress about 159-62-6. 159-62-6 belongs to naphthyridine, auxiliary class Other Aromatic Heterocyclic,Spiro, name is Spiro[fluorene-9,9′-xanthene], and the molecular formula is C25H16O, SDS of cas: 159-62-6.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem

Wu, Haibo’s team published research in Journal of Separation Science in 35 | CAS: 2960-93-2

Journal of Separation Science published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C7H7BF2O3, Application of 2,2′-Dimethoxy-1,1′-binaphthalene.

Wu, Haibo published the artcileInvestigation of brush-type chiral stationary phases based on O,O’-diaroyl tartardiamide and O,O’-bis-(arylcarbamoyl) tartardiamide, Application of 2,2′-Dimethoxy-1,1′-binaphthalene, the publication is Journal of Separation Science (2012), 35(3), 351-358, database is CAplus and MEDLINE.

Four chiral organosilanes based on O,O’-dibenzoyl tartardiamide, O,O’-bis-(3,5-dimethylbenzoyl) tartardiamide, O,O’-bis-(phenylcarbamoyl) tartardiamide and O,O’-bis-[(3,5-dimethylphenyl)carbamoyl] tartardiamide were synthesized and immobilized on silica to afford corresponding brush-type chiral stationary phases (CSPs) with well-defined structures. Using 54 compounds containing a wide variety of structures as analytes, the enantioselectivities of the four CSPs were evaluated under normal-phase modes. 3,5-Di-Me substituent in the aryl group was found to significantly affect the enantioselectivity of CSPs containing aryl ester moieties. Aryl carbamate moieties in CSPs were observed more beneficial for enantioseparation than aryl ester moieties. The addnl. hydrogen-bond donors (NH) present in the carbamate groups contributed greatly to the enantioselectivity of CSPs, which is contrary to the results that were found in network-polymeric CSPs.

Journal of Separation Science published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C7H7BF2O3, Application of 2,2′-Dimethoxy-1,1′-binaphthalene.

Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem