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Denise A Colby

Publications and source records attributed to Denise A Colby.

8 recordsLinked to original sources
PubMed2006

Stereoselective alkylation of alpha,beta-unsaturated imines via C-H bond activation.

The stereoselective alkylation of alpha,beta-unsaturated imines via C-H activation followed by imine hydrolysis produces tri- and tetrasubstituted alpha,beta-unsaturated aldehydes. In the presence of a rhodium catalyst, alpha,beta-unsaturated N-benzyl imines derived from methacrolein, crotonaldehyde, and tiglic aldehyde undergo directed C-H activation at the beta-position and react with terminal alkenes and alkynes to form the tri- and tetrasubstituted alpha,beta-unsaturated imines with very high stereoselectivity. Hydrolysis to provide alpha,beta-unsaturated aldehydes can be performed under carefully controlled conditions that maintain the stereochemistry of the beta-alkylated imine products. Alternatively, for beta-alkylation products of the N-benzyl imine of methacrolein, hydrolysis can be performed under conditions that provide complete isomerization to the E isomer.

Alkylation↗
PubMed2004

Synthesis, spectroscopy, and reactivity of meso-unsubstituted azuliporphyrins and their heteroanalogues. Oxidative ring contractions to carba-, oxacarba-, thiacarba-, and selenacarbaporphyrins.

This paper reports the first detailed study on meso-unsubstituted azuliporphyrins, an important family of porphyrin-like molecules where one of the usual pyrrole rings has been replaced by an azulene subunit. Although the azulene moiety introduces an element of cross-conjugation, zwitterionic resonance contributors with tropylium and carbaporphyrin substructures give azuliporphyrins diatropic character that falls midway between true carbaporphyrins and nonaromatic benziporphyrins. Protonation affords an aromatic dication where this type of resonance interaction is favored due to the associated charge delocalization. Two different "3 + 1" syntheses of meso-unsubstituted azuliporphyrins have been developed. Acid-catalyzed reaction of readily available tripyrrane dicarboxylic acids with 1,3-azulenedicarbaldehyde, followed by oxidation with DDQ or FeCl(3), affords good yields of azuliporphyrins. Alternatively, azulene reacted with acetoxymethylpyrroles (2 equiv) in refluxing acetic acid/2-propanol to give tripyrrane analogues, and following a deprotection step, condensation with a pyrrole dialdehyde in TFA-CH(2)Cl(2) gave the azuliporphyrin system. The latter approach was also used to prepare 23-thia- and 23-selenaazuliporphyrins. However, reaction of the azulitripyrrane with 2,5-furandicarbaldehyde produced a mixture of three oxacarbaporphyrins in moderate yield. The free base forms of thia- and selenaazuliporphyrins both showed intermediary aromatic character that was considerably enhanced upon protonation. The UV-vis spectra for azuliporphyrins and their heteroanalogues showed four bands between 350 and 500 nm and broad absorptions at higher wavelengths. Addition of TFA gave dications that showed porphyrin-like spectra with Soret bands between 460 and 500 nm. In the presence of pyrrolidine, azuliporphyrins and their heteroanalogues undergo nucleophilic attack on the seven-membered ring to give carbaporphyrin adducts. These systems also undergo oxidative rearrangements under basic conditions with t-BuOOH to give benzocarbaporphyrins. The selenaazuliporphyrin afforded two benzoselenacarbaporphyrins, a previously unknown core-modified carbaporphyrin system. The proton NMR spectra for these compounds showed strong diatropic ring currents with the internal CH resonance upfield above -5 ppm, while the meso-protons resonated downfield near 10 ppm. The UV-vis spectra were also porphyrin-like and gave strong Soret bands at ca. 440 nm.

Acids↗
PubMed2004

New riches in carbaporphyrin chemistry: silver and gold organometallic complexes of benzocarbaporphyrins.

The NH-N-NH-N core of the porphyrin system represents one of the best studied and most versatile platforms for coordination chemistry. However, the replacement of one or more of the interior nitrogens with carbon atoms would be expected to diminish the ability of these systems to form metallo derivatives considerably. Despite this expectation, carbaporphyrinoid systems have been shown to form stable organometallic derivatives. Although azuliporphyrins and benziporphyrins act as dianionic ligands, benzocarbaporphyrins are trianionic ligands. Treatment of five different meso unsubstituted benzocarbaporphyrins and two different meso tetraarylbenzocarbaporphyrins with excess silver(I) acetate afforded 65-97% yields of the corresponding silver(III) organometallic derivatives. The insertion of silver metal was confirmed by mass spectrometry and X-ray crystallography. The UV-vis spectra showed a strong Soret band at wavelengths between 437 and 451 nm, together with a series of Q-type bands at longer wavelengths. The new metallo carbaporphyrins demonstrate the presence of a strong diatropic ring current in their proton NMR spectra, and carbon-13 NMR spectroscopy indicates that the derivatives retain a plane of symmetry. The reaction of meso tetraaryl carbaporphyrins with gold(III) acetate afforded the related gold(III) complexes, and these also showed strongly porphyrin-like aromatic characteristics. The UV-vis spectra for the gold complexes again showed a strong Soret band between 437-439 nm, but a secondary band near 400 nm is somewhat intensified for the gold species compared to the spectra for the related silver(III) meso tetrasubstituted carbaporphyrins. The ring currents observed for the gold(III) complexes by proton NMR spectroscopy were comparable to those of the silver(III) derivatives, implying that both series have similar macrocyclic conformations. Cyclic voltammetry was performed on two different carbaporphyrins, their silver(III) derivatives, and a gold(III) complex. The silver complexes display a reversible cathodic wave that is assigned to the Ag(III/II) couple. However, the gold porphyrinoid gave a value for the reductive wave that could be due to a gold(III/II) couple or a ligand-based process.

Journal Article↗
PubMed2003

Organometallic chemistry of azuliporphyrins: synthesis, spectroscopy, electrochemistry, and structural characterization of nickel(II), palladium(II), and platinum(II) complexes of azuliporphyrins.

Four azuliporphyrins, two meso-unsubstituted and two meso-tetraaryl substituted, were investigated in the synthesis of novel organometallic compounds. The meso-unsubstituted or "etio" series azuliporphyrins 8 reacted with nickel(II) acetate, palladium(II) acetate, and platinum(II) chloride in DMF to give the corresponding chelates 14-16, where the metal cation lies within the macrocyclic cavity and binds to all three nitrogens and the internal carbon atom. The newly available meso-tetraarylazuliporphyrins 13 similarly afforded the corresponding nickel(II), palladium(II), and platinum(II) complexes, 17-19, respectively. The new organometallic complexes are stable nonpolar compounds and were fully characterized spectroscopically and by mass spectrometry. The UV-vis data indicate that these complexes, in common with the parent azuliporphyrin system 8, do not possess porphyrin-type aromaticity. However, electron donation from the azulene unit can give rise to dipolar resonance contributors that provide a degree of carbaporphyrin-type aromatic character. The platinum(II) azuliporphyrins 16 gave noteworthy proton NMR spectra where the meso-protons showed satellite peaks due to transannular coupling to platinum-195. The pyrrolic protons of the platinum(II) meso-tetraarylazuliporphyrin 19b also showed similar satellite peaks due to coupling from the platinum-195 isotope. The electrochemistry of free base tetraphenylazuliporphyrin 13a and the related nickel(II) and palladium(II) complexes was investigated using cyclic voltammetry, and these data indicate that metal coordination improves the reversibility of the ligand-based oxidations. Nickel(II) azuliporphyrin 14a and palladium(II) tetrakis(4-chlorophenyl)azuliporphyrin 18b were also structurally characterized by X-ray crystallography. The macrocyclic core of the palladium(II) complex 18b was significantly more planar than the nickel(II) derivative 14b, and this difference was attributed to the better size match between the azuliporphyrin cavity and the larger palladium(II) ion. The straightforward synthesis of metalloazuliporphyrins under mild conditions, and their interesting spectroscopic, electrochemical, and structural features, demonstrates that the azuliporphyrin system holds great promise as a platform for organometallic chemistry.

Journal Article↗
PubMed2002

Adaptation of the Rothemund reaction for carbaporphyrin synthesis: preparation of meso-tetraphenylazuliporphyrin and related benzocarbaporphyrins.

Electrophilic substitution of azulene has recently been shown to provide the means by which carbon-carbon bonds can be generated to form novel macrocyclic systems such as calixazulenes. These studies inspired us to develop a "one-pot" Rothemund-type synthesis of meso-tetraphenylazuliporphyrin. Azuliporphyrins, a group of cross-conjugated carbaporphyrinoids that exhibit intriguing chemistry and metallation properties, have previously only been available by multistep syntheses. In this work, azulene, pyrrole and benzaldehyde were shown to react in a 1:3:4 ratio in the presence of boron trifluoride etherate to give meso-tetraphenylazuliporphyrin 7a. The free base shows only a minor diatropic ring current, but addition of TFA generates the related dication which shows greatly enhanced diatropicity where the internal CH shifts from delta = +3.35 to -0.5 ppm. Addition of pyrrolidine to 7a gave rise to a carbaporphyrin adduct which showed a porphyrin-like UV/Vis spectrum and the internal CH shifted further upfield to give a resonance near delta = -5.7 ppm. Treatment of 7a with tertbutyl hydroperoxide in the presence of potassium hydroxide afforded a mixture of benzocarbaporphyrins 9a-c. These tetraphenylcarbaporphyrins were fully aromatic by NMR spectroscopy and gave typical porphyrin-type UV/Vis spectra with a strong Soret band near 446 nm. This new methodology makes these important porphyrin analogues readily available for further study.

Journal Article↗
PubMed2002

Calix[4]azulene.

Azulene reacts with paraformaldehyde in the presence of florisil to give excellent yields of calix[4]azulene.

Journal Article↗