Abstract:An overview of most of the well known rhenium porphyrins is presented reviewing their synthesis, coordination chemistry, and applications. The chemistry of some recently known porphyrin-Re conjugates is also discussed.
“…11 Porphyrins as electron-rich organic molecules are characterized by remarkably high extinction coefficients in the visible region. 12,13 They are one of the most promising components of new materials for future electronic devices. For example, meso-tetra (4-sulfonatophenyl) porphyrin (H 2 TPPS 4 ), a water-soluble porphyrin with hydrophily grounds and light-harvesting capacity, 14 is beneficial to using photocatalytic synthesis to prepare novel materials with specific features.…”
Photochemical synthesis under visible irradiation is a novel approach in the field of green chemistry, and composites with abundant active centers for electrochemical detection are greatly attractive. Herein, meso-tetra (4-sulfonatophenyl)...
“…11 Porphyrins as electron-rich organic molecules are characterized by remarkably high extinction coefficients in the visible region. 12,13 They are one of the most promising components of new materials for future electronic devices. For example, meso-tetra (4-sulfonatophenyl) porphyrin (H 2 TPPS 4 ), a water-soluble porphyrin with hydrophily grounds and light-harvesting capacity, 14 is beneficial to using photocatalytic synthesis to prepare novel materials with specific features.…”
Photochemical synthesis under visible irradiation is a novel approach in the field of green chemistry, and composites with abundant active centers for electrochemical detection are greatly attractive. Herein, meso-tetra (4-sulfonatophenyl)...
“…Several classes of rhenium based radiopharmaceuticals exists varying from small molecules, colloids, peptides to antibodies, each of which are coordinated or labelled differently with the rhenium metal centre and are distributed in various ways through the body to the potential disease site, whether it is cancer, arthritis, etc. all of which speaks to the versatility of rhenium-based radiopharmaceuticals [11,12]. Aside from the direct use of the radioactive isotope, the nonradioactive rhenium can be used as a chemical analogue to the short-lived isotope of technetium namely, 99m Tc, which is widely used in the medicinal world today [13].…”
“…In summary, the high-temperature interaction of Re 2 (CO) 10 with three free-base meso -triarylcorroles has led to the isolation of neutral rhenium corrole sandwich compounds with the molecular formula ReH[T p XPC] 2 , a heretofore unprecedented coordination motif in the field of rhenium–porphyrinoid interactions. , DFT calculations and Re L 3 -edge EXAFS studies support a seven-coordinate rhenium center and one loosely interacting NH group. The extra hydrogen can be removed by a base, resulting in dramatically sharper UV–vis spectra consistent with C 2 -symmetric {Re[T p XPC] 2 } − anions.…”
mentioning
confidence: 92%
“…The interaction of rhenium with porphyrin-type ligands has resulted in a growing variety of coordination motifs in recent years. , Thus, porphyrins and related ligands (such as sapphyrin , and triphyrin) act as tridentate ligands toward the [Re(CO) 3 ] + fragment to yield unusual “capped” organometallic complexes that obey the 18-electron rule. Likewise, 99 Tc(CO) 3 -capped porphyrin derivatives are also well-known .…”
The interaction of three free-base meso-tris(p-X-phenyl)corroles H3[TpXPC]
(X = H, CH3, OCH3) with Re2(CO)10 at 235 °C in the presence of K2CO3 in o-dichlorobenzene has led to putative rhenium
biscorrole sandwich compounds with the formula ReH[TpXPC]2. Density functional theory calculations and Re L3-edge extended X-ray absorption fine structure measurements
suggest a seven-coordinate metal center, with the “extra”
hydrogen located on one of the corrole nitrogens. The complexes can
be deprotonated by a base such as 1,8-diazabicyclo[5.4.0]undec-7-ene,
resulting in a substantial sharpening of the UV–vis spectra
and split Soret bands, consistent with the generation of C
2-symmetric anions. Both the seven-coordinate neutral
and eight-coordinate anionic forms of the complexes represent a new
coordination motif in the field of rhenium–porphyrinoid interactions.
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