Chhanda, Sadia Afrin et al. published their research in Journal of Catalysis in 2019 |CAS: 144970-30-9

The Article related to cinchona squaramide iodoarene copolymer preparation recyclability, keto ester nitro vinylarene chiral polymer organocatalyst michael addition, alkyl aryl nitroalkyl oxo cyclopentanecarboxylate diastereoselective enantioselective preparation and other aspects.Computed Properties of 144970-30-9

On September 30, 2019, Chhanda, Sadia Afrin; Itsuno, Shinichi published an article.Computed Properties of 144970-30-9 The title of the article was Design and synthesis of chiral hyperbranched polymers containing cinchona squaramide moieties and their catalytic activity in the asymmetric Michael addition reaction. And the article contained the following:

Chiral hyperbranched polymers (HBP) containing cinchona alkaloids were synthesized using a Mizoroki-Heck (MH) coupling polymerization reaction between a cinchona squaramide dimer and tri- or tetra-substituted aromatic iodides. This was a new type of polymeric chiral organocatalyst. We found that the as-obtained chiral HBPs show excellent catalytic activity in the asym. Michael reaction. Almost perfect enantioselectivity (>99% ee) was achieved in the reaction of β-ketoester and trans-β-nitrostyrene. The three-dimensional network structure of the chiral HBPs is structurally robust and can be reused for further reaction without any loss in their catalytic activity. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Computed Properties of 144970-30-9

The Article related to cinchona squaramide iodoarene copolymer preparation recyclability, keto ester nitro vinylarene chiral polymer organocatalyst michael addition, alkyl aryl nitroalkyl oxo cyclopentanecarboxylate diastereoselective enantioselective preparation and other aspects.Computed Properties of 144970-30-9

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Wei, Qian et al. published their research in Tetrahedron in 2004 |CAS: 144970-30-9

The Article related to ruthenium tripodal sensitizer conjugated nonconjugated bridge preparation fluorescence, conjugation effect ruthenium tripodal sensitizer rigid rod bridge, photophys ruthenium tripodal sensitizer conjugated nonconjugated bridge and other aspects.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

On September 13, 2004, Wei, Qian; Galoppini, Elena published an article.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane The title of the article was Tripodal Ru(II) complexes with conjugated and non-conjugated rigid-rod bridges for semiconductor nanoparticles sensitization. And the article contained the following:

Three tripodal Ru(II)-polypyridyl complexes were synthesized as models to study long-range electron transfer in TiO2 semiconductor nanoparticle thin films, in particular to study the effect of the conjugation of the bridge containing the Ru complex and for distance-dependence studies. The tripodal sensitizers, which are 1,3,5,7-tetraphenyladamantane derivatives having three COOMe anchoring groups and one rigid-rod bridge substituted with a Ru(II) complex, are the longest prepared to date (Ru-to-footprint distance ∼24 Å). Two have a rigid-rod bridge made of two p-ethynylphenylene units (Ph-E)2 capped with a 4-(2,2′-bipyridyl) (bpy) ligand or a 5-(1,10-phenanthrolinyl) (phen) ligand for the Ru complex. The third tripod, which contains a bpy ligand for the Ru complex, has one bicyclo[2.2.2]octylene (Bco) unit in place of a p-phenylene (Ph) unit and is the first example of a tripodal sensitizer with a nonconjugated bridge. Solution absorption and fluorescence data of the three complexes are reported. Photophys. studies of the non-conjugated Bco-bridged complex on TiO2 are not reported. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

The Article related to ruthenium tripodal sensitizer conjugated nonconjugated bridge preparation fluorescence, conjugation effect ruthenium tripodal sensitizer rigid rod bridge, photophys ruthenium tripodal sensitizer conjugated nonconjugated bridge and other aspects.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Li, Quan et al. published their research in Organic Letters in 2002 |CAS: 144970-30-9

The Article related to tetrahedral arylalkyne preparation single mol afm probe tip, iodophenylmethane iodophenyladamantane preparation, sonogashira coupling reaction alkynylarylazadithiepine, afm imaging azathiepinylethynylphenylethynylphenylmethane and other aspects.Category: iodides-buliding-blocks

On October 17, 2002, Li, Quan; Rukavishnikov, Aleksey V.; Petukhov, Pavel A.; Zaikova, Tatiana O.; Keana, John F. W. published an article.Category: iodides-buliding-blocks The title of the article was Nanoscale 1,3,5,7-Tetrasubstituted Adamantanes and p-Substituted Tetraphenyl-methanes for AFM Applications. And the article contained the following:

Tetrahedrally shaped mols.such as I based on tetrasubstituted methane or tetrasubstituted adamantane cores are prepared as potential precursors for single-mol. AFM tips. 1,3,5,7-Tetra(4-iodophenyl)adamantane is prepared in two steps from 1-bromoadamantane and benzene by heating with tert-Bu bromide and aluminum chloride followed by electrophilic iodination; the corresponding tetra(4-iodophenyl)methane is prepared from 4-tritylaniline by diazotization and substitution with iodide followed by electrophilic iodination. N-alkynylaryldithiazepane building blocks are prepared from 4-iodoaniline by addition of ethylene oxide, chlorination of the 2-hydroxyethylamino substituents, conversion via the bisthiocyanate to the dithiazepane, Sonogashira coupling reaction of the aryl iodide moiety with trimethylsilylacetylene and desilylation, coupling with 4-iodophenylethynyltrimethylsilane, and desilylation to provide the arms of I in seven steps. Sonogashira coupling of tetra(4-iodophenyl)methane with the arm unit yields I. AFM images of I indicate that I can be imaged with a conventional AFM tip. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Category: iodides-buliding-blocks

The Article related to tetrahedral arylalkyne preparation single mol afm probe tip, iodophenylmethane iodophenyladamantane preparation, sonogashira coupling reaction alkynylarylazadithiepine, afm imaging azathiepinylethynylphenylethynylphenylmethane and other aspects.Category: iodides-buliding-blocks

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Boldog, Ishtvan et al. published their research in CrystEngComm in 2013 |CAS: 144970-30-9

The Article related to manganese lanthanum tetrazolate phosphonate tetraphenyladamantane complex preparation crystal structure, magnetic property manganese lanthanum tetrazolate phosphonate functionalized tetraphenyladamantane complex and other aspects.Recommanded Product: 144970-30-9

Boldog, Ishtvan; Domasevitch, Konstantin V.; Baburin, Igor A.; Ott, Holger; Gil-Hernandez, Beatriz; Sanchiz, Joaquin; Janiak, Christoph published an article in 2013, the title of the article was A rare alb-4,8-Cmce metal-coordination network based on tetrazolate and phosphonate functionalized 1,3,5,7-tetraphenyladamantane.Recommanded Product: 144970-30-9 And the article contains the following content:

Sym. tetrahedral ligands are prominent, but somewhat under-studied building blocks for the generation of coordination polymeric networks. Coordination networks [Mn5Cl2(L1)2(H2O)4(DMF)4]·3H2O·7DMF, 1 and the [La2(H5L2)2(H2O)6], 2 were synthesized under mild solvothermal methods in DMF from the adamantane-based tetrahedral ligands, 1,3,5,7-tetrakis(4-phenyltetrazol-5-yl)adamantane (H4L1), reported for the first time, and 1,3,5,7-tetrakis(4-phenylphosphonic acid)adamantane (H8L2), resp. Compounds 1 and 2 are based on completely different pentanuclear and binuclear secondary metal building units, resp., and have different symmetries, but demonstrate an interesting coincidence of underlying topologies, which could be interpreted as a directing or imprinting’ effect of the symmetry of the rigid tetrahedral ligands. Both structures represent examples of a rarely observed (4,8)-coordinated net. The χMT product for 1 at room temperature is slightly lower than the expected for five Mn(II) ions with S = 5/2 and g ≈ 1.98 and on lowering the temperature χMT approaches the expected value for a single Mn(II) as a result of the antiferromagnetic coupling through the tetrazolate bridges. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Recommanded Product: 144970-30-9

The Article related to manganese lanthanum tetrazolate phosphonate tetraphenyladamantane complex preparation crystal structure, magnetic property manganese lanthanum tetrazolate phosphonate functionalized tetraphenyladamantane complex and other aspects.Recommanded Product: 144970-30-9

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Dohi, Toshifumi et al. published their research in Chemical & Pharmaceutical Bulletin in 2006 |CAS: 144970-30-9

The Article related to pyrrole cyanation silyl cyanide recyclable hypervalent iodine reagent, thiophene cyanation silyl cyanide recyclable hypervalent iodine reagent, cyano heteroaromatic compound pyrrole thiophene preparation and other aspects.Application of 144970-30-9

On November 30, 2006, Dohi, Toshifumi; Morimoto, Koji; Takenaga, Naoko; Maruyama, Akinobu; Kita, Yasuyuki published an article.Application of 144970-30-9 The title of the article was A facile and clean direct cyanation of heteroaromatic compounds using a recyclable hypervalent iodine(III) reagent. And the article contained the following:

The facile and clean direct cyanating reaction of pyrroles and thiophenes was achieved using a recyclable hypervalent iodine(III) reagent by a simple solid-liquid separation of the products and the reagent. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Application of 144970-30-9

The Article related to pyrrole cyanation silyl cyanide recyclable hypervalent iodine reagent, thiophene cyanation silyl cyanide recyclable hypervalent iodine reagent, cyano heteroaromatic compound pyrrole thiophene preparation and other aspects.Application of 144970-30-9

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Lee, Chi-Hang et al. published their research in Tetrahedron in 2010 |CAS: 144970-30-9

The Article related to bipyridineethynylphenyladamantane carboxylate derivative preparation ruthenium complex, electrochem ruthenium bipyridineethynylphenyladamantane carboxylic ester complex, fluorescence ruthenium bipyridineethynylphenyladamantane carboxylic acid complex, quenching fluorescence ruthenium bipyridineethynylphenyladamantane carboxylic acid titanium dioxide and other aspects.Computed Properties of 144970-30-9

On May 29, 2010, Lee, Chi-Hang; Zhang, Yongyi; Romayanantakit, Apiwat; Galoppini, Elena published an article.Computed Properties of 144970-30-9 The title of the article was Modular synthesis of ruthenium tripodal system with variable anchoring groups positions for semiconductor sensitization. And the article contained the following:

The authors describe an improved synthetic approach to access tripodal compounds with variable footprints and anchor groups. Two Ru(II) bipyridine tripodal complexes with three carboxylic acid groups in meta (Ru-m-COOH, 1; I) and para (Ru-p-COOH, 2; II) positions, and with large (180-250 Å2) footprints were synthesized and bound to the surface of nanostructured TiO2. Selected properties of 1 and 2 in solution and bound are reported. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Computed Properties of 144970-30-9

The Article related to bipyridineethynylphenyladamantane carboxylate derivative preparation ruthenium complex, electrochem ruthenium bipyridineethynylphenyladamantane carboxylic ester complex, fluorescence ruthenium bipyridineethynylphenyladamantane carboxylic acid complex, quenching fluorescence ruthenium bipyridineethynylphenyladamantane carboxylic acid titanium dioxide and other aspects.Computed Properties of 144970-30-9

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Galoppini, Elena et al. published their research in Journal of the American Chemical Society in 2002 |CAS: 144970-30-9

The Article related to electron transfer across mol nanocrystalline semiconductor interface tripodal photosensitizer, safety photoinduced electron transfer titania tripodal ruthenium complex sensitizer, zirconia tripodal ruthenium complex sensitizer interfacial photoinduced electron transfer and other aspects.Recommanded Product: 144970-30-9

On July 3, 2002, Galoppini, Elena; Guo, Wenzhuo; Zhang, Wei; Hoertz, Paul G.; Qu, Ping; Meyer, Gerald J. published an article.Recommanded Product: 144970-30-9 The title of the article was Long-range electron transfer across molecule-nanocrystalline semiconductor interfaces using tripodal sensitizers. And the article contained the following:

Four tripodal sensitizers, Ru(bpy)2(Ad-tripod-phen)2+ (1), Ru(bpy)2(Ad-tripod-bpy)2+ (2), Ru(bpy)2(C-tripod-phen)2+ (3), and Ru(bpy)2(C-tripod-bpy)2+ (4) (bpy = 2,2′-bipyridine; phen = 1,10-phenanthroline; Ad-tripod-bpy (phen) and C-tripod-bpy (phen) = tripod-shaped bpy (phen) ligands based on 1,3,5,7-tetraphenyladamantane and tetraphenylmethane, resp.), have been synthesized and characterized. The tripodal sensitizers consist of a rigid-rod arm linked to a RuII-polypyridine complex at one end and three COOR groups on the other end that bind to metal oxide nanoparticle surfaces. The excited-state and redox properties of solvated and surface-bound 1-4 have been studied at room temperature The absorption spectra, emission spectra, and electrochem. properties of 1-4 in acetonitrile solution are preserved when 1-4 are bound to nanocrystalline (anatase) TiO2 or colloidal ZrO2 mesoporous films. This behavior is indicative of weak electronic coupling between TiO2 and the sensitizer. The kinetics for excited-state decay are exponential for 1-4 in solution and are nonexponential when 1-4 are bound to ZrO2 or TiO2. Efficient and rapid (kcs > 108 s-1) excited-state electron injection is observed for 1-4/TiO2. The recombination of the injected electron with the oxidized RuIII center is well described by a second-order kinetic model with rate constants that are independent of the sensitizer. The sensitizers bound to TiO2 were reversibly oxidized electrochem. with an apparent diffusion coefficient ∼1 × 10-11 cm2-s-1. Caution preparation of diazomethane (in synthesis of reactant for preparation tripodal ligand) was done in special glassware with smooth joints following safety precautions. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Recommanded Product: 144970-30-9

The Article related to electron transfer across mol nanocrystalline semiconductor interface tripodal photosensitizer, safety photoinduced electron transfer titania tripodal ruthenium complex sensitizer, zirconia tripodal ruthenium complex sensitizer interfacial photoinduced electron transfer and other aspects.Recommanded Product: 144970-30-9

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Patil, Komal M. et al. published their research in Crystal Growth & Design in 2016 |CAS: 144970-30-9

The Article related to preparation diamondoid lonsdaleite network silver cyanophenyladamantane network complex, crystal structure diamondoid lonsdaleite network silver cyanophenyladamantane network complex, thermal decomposition diamondoid lonsdaleite network silver cyanophenyladamantane network complex and other aspects.Category: iodides-buliding-blocks

On February 3, 2016, Patil, Komal M.; Dickinson, Michelle E.; Tremlett, Thomas; Moratti, Stephen C.; Hanton, Lyall R. published an article.Category: iodides-buliding-blocks The title of the article was Synthesis of Diamondoid and Lonsdaleite Networks from the Same Ag(I)-Ligand Combination, with Lonsdaleite the Softer Network. And the article contained the following:

The design and synthesis of a Lonsdaleite (lon) network is an attractive and challenging supramol. target. The authors’ reticular synthesis strategy of slow diffusion of solutions of a simple rigid tetrahedral ligand and a Ag(I) metal ion, at room temperature and atm. pressure, resulted in both lon-MOFs and diamondoid (dia-MOFs) and associated 2D honeycomb networks. The prepared complexes are {[AgL]X.nCH3NO2} [X = CF3SO3-, n = 4 (1a, 1); BF4-, n = 3 (1b, 2); CF3CO2-, n = 5.5 (1c, 3); BF4-, n = 4 (1d, 4)] and interpenetrated dia {[AgL]X.nH2O} [X = PF6-, n = 2 (2a, 5); BF4-, n = 3 (2b, 6); ClO4-, n = 2 (2c, 7), CF3SO3- (2d, 8)] networks along with their associated 2D honeycomb (hcb) networks {[AgL](CF3SO3).2CH3NO2.H2O} (3a, 9) and {[AgL(NO3)].4CH3NO2.H2O} (3b, 10) (where L = tetrakis(4-cyanophenyl)adamantane). Solvent appeared to play a key role in templating the formation of these related networks. Nanoindentation studies show that a dia-MOF was 42% harder than a lon-MOF counterpart. The lon-MOFs were thermally stable and retained integrity until 370° while dia-MOFs exhibited stepwise collapse after initial loss of solvents. As lon networks are often only qual. identified, Cremer-Pople ring puckering anal. was used to quantify the degree of distortion in the lon and related 4-connected 66 networks. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Category: iodides-buliding-blocks

The Article related to preparation diamondoid lonsdaleite network silver cyanophenyladamantane network complex, crystal structure diamondoid lonsdaleite network silver cyanophenyladamantane network complex, thermal decomposition diamondoid lonsdaleite network silver cyanophenyladamantane network complex and other aspects.Category: iodides-buliding-blocks

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Tohma, Hirofumi et al. published their research in Angewandte Chemie, International Edition in 2004 |CAS: 144970-30-9

The Article related to tetrakisdiacetoxyiodophenyladamantane recyclable oxidizing agent preparation, recyclable hypervalent iodine reagent preparation, diacetoxyiodophenyladamantane tetrakis recyclable oxidizing agent preparation, adamantane tetrakisdiacetoxyiodophenyl recyclable oxidizing agent preparation and other aspects.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

On July 5, 2004, Tohma, Hirofumi; Maruyama, Akinobu; Maeda, Akihisa; Maegawa, Tomohiro; Dohi, Toshifumi; Shiro, Motoo; Morita, Tetsuichiro; Kita, Yasuyuki published an article.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane The title of the article was Preparation and reactivity of 1,3,5,7-tetrakis[4-(diacetoxyiodo)phenyl]adamantane, a recyclable hypervalent iodine(III) reagent. And the article contained the following:

A wide range of oxidative reactions are mediated by novel, nonpolymeric, and recyclable hypervalent IIII reagents [e.g. I, R = I(OAc)2]. In all cases, tetraiodide I (R = I) was recovered nearly quant. in pure form after a simple workup. Reoxidation of I (R = I) to I [R = I(OAc)2] with m-chloroperbenzoic acid also proceeded quant., without loss of oxidative activity. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

The Article related to tetrakisdiacetoxyiodophenyladamantane recyclable oxidizing agent preparation, recyclable hypervalent iodine reagent preparation, diacetoxyiodophenyladamantane tetrakis recyclable oxidizing agent preparation, adamantane tetrakisdiacetoxyiodophenyl recyclable oxidizing agent preparation and other aspects.Name: 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Reichert, Veronica R. et al. published their research in Macromolecules in 1994 |CAS: 144970-30-9

The Article related to tetraphenyladamantane derivative preparation dendrimer preparation modeling, polyphenylene dendrimer preparation model tetramethyladamantane derivative, core tetraphenyladamantane derivative polyamide polyphenylene dendrimer, polyamide dendrimer preparation model tetramethyladamantane derivative and other aspects.Application In Synthesis of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

On November 21, 1994, Reichert, Veronica R.; Mathias, Lon J. published an article.Application In Synthesis of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane The title of the article was Expanded Tetrahedral Molecules from 1,3,5,7-Tetraphenyladamantane. And the article contained the following:

The goal of this paper was to investigate the effects of rigid tetrahedral cores (such as adamantane) on the properties of aramid and poly(phenylene) dendrimers as well as dendrimers that form single mol. micelles. This paper deals with model compound studies dealing with generating tetrasubstituted derivatives of adamantane. A previously reported procedure (for making tetraphenyladamantane) using tert-Bu bromide-AlCl3 catalyzed arylation of 1-bromoadamantane was found not to be a general synthetic method for the preparation of other substituted adamantane derivatives Adamantane derivatives with multiple Ph substituents were isolated only when benzene and bromobenzene were used in the Friedel-Crafts reaction. Tetraphenyl-substituted adamantane derivatives were formed, however, by the traditional Friedel-Crafts arylation of 1,3,5,7-tetrabromoadamantane with bromobenzene and 1,3-dibromobenzene. A lack of regioselectivity for these reactions (isolated mixtures of the meta/para isomers or ortho/meta isomers) was observed Large quantities (50-100 g) of 1,3,5,7-tetraphenyladamantane (1) were prepared from 1-bromoadamantane using a slightly modified literature procedure. This organic insoluble compound was iodinated with [bis(trifluoroacetoxy)iodo]benzene to give the all-para-substituted compound, 5. Compound 5 was further reacted to give numerous derivatives and used as a core in the synthesis of first generation dendrimers. The experimental process involved the reaction of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane(cas: 144970-30-9).Application In Synthesis of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

The Article related to tetraphenyladamantane derivative preparation dendrimer preparation modeling, polyphenylene dendrimer preparation model tetramethyladamantane derivative, core tetraphenyladamantane derivative polyamide polyphenylene dendrimer, polyamide dendrimer preparation model tetramethyladamantane derivative and other aspects.Application In Synthesis of 1,3,5,7-Tetrakis(4-iodophenyl)adamantane

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com