Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorum

[reaction: see text] Two new neoclerodane diterpenes, salvinicins A (4) and B (5), were isolated from the dried leaves of Salvia divinorum. The structures of these compounds were elucidated by spectroscopic techniques, including (1)H and (13)C NMR, NOESY, HMQC, and HMBC. The absolute stereochemistry of these compounds was assigned on the basis of single-crystal X-ray crystallographic analysis of salvinicin A (4) and a 3,4-dichlorobenzoate derivative of salvinorin B.     

Organotin(IV) Complexes of 2-[(2′,4′,6′- Trichlorophenylamido)]benzoic Acid: Synthesis,Coordination Chemistry,and Semi-Empirical Study

A new series of organotin(IV) complexes of aniline derivatives, R₂SnL₂ and R₃SnL [where R = Me, n-Bu, n-Oct, and Ph], have been synthesized by the reaction of ligand acid with respective organotin halides in the presence of triethylamine as base or dioctyltin oxide using a Dean–Stark trap for the removal of water under reflux conditions. Experimental details for the preparation and characterization, including elemental analysis, IR, semi-empirical study, multinuclear NMR (¹H, ¹³C, and ¹¹⁹Sn spectra and EI mass spectral studies) of all reported complexes are provided. The IR data indicate that in both di- and triorganotin(IV) carboxylates, the ligand moiety ?COO acts as a bidentate group in the solid state. Multinuclear NMR data show that triorganotin complexes exhibits a four-coordinated geometry, while diorganotin(IV) complexes show a coordination number greater than four, probably five or six, in solution state.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.     

Synthesis,Characterization, and Semi-Empirical Study of Organotin(IV) Complexes with 4-(Hydroxymethyl)piperidine-1-carbodithioic Acid: X-Ray Structure of Chlorodimethyl-(4-hydroxymethyl piperidine-1-carbodithioato-S,S′)tin(IV)

Abstract

Organotin complexes with the general formulae R₂SnL₂, R₂Sn(Cl)L, and R₃SnL have been synthesized where R = CH₃, n-C₄H₆, C₆H₅, C₆H₁₁, and L = 4-(hydroxy methyl)piperidine-1-carbodithioic acid. The newly synthesized complexes have been characterized by elemental analysis, IR, NMR (¹H, ¹³C and ¹¹⁹Sn), and, for one example, a single crystal x-ray structure. The FT-IR data shows the bidentate nature of the ligand. This coordination behavior is also confirmed by semi-empirical study. In the solid state, diorganotin complexes exhibit the penta/hexacoordinated geometry, whereas the triorganotin(IV) complexes show the five coordinated geometry. ¹¹⁹Sn NMR data reveal that triorganotin(IV) complexes exhibit the four coordinated geometry in solution, whereas the diorganotin(IV) compounds show the higher coordination, probably five or six. X-ray diffraction analysis of complex (2) shows a square pyramidal geometry around the tin atom on the basis of τ value.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

GRAPHICAL ABSTRACT      

Synthesis, characterization, and biological activities of homo- and heterobimetallic complexes of Sn(IV) and Pd(II) with 2-mercapto-5-methyl benzimidazole

Organotin complexes have been synthesized by refluxing 2-mercapto-5-methyl benzimidazole with R₂SnCl₂/R₃SnCl (R = Me, n-Bu, Ph) in 1:1 molar ratio in the first step. In the second step, synthesized organotin(IV) complexes were treated with CS₂ and R₂SnCl₂/R₃SnCl/PdCl₂ to yield homo- and heterobimetallic complexes. The composition of the synthesized complexes, the bonding behavior of the donor groups, and structural assignments were studied by elemental analysis and different spectral techniques, including IR and multinuclear NMR (¹H, ¹³C). The IR data shows bidentate nature of the ligand which is also confirmed by semiempirical study, while NMR data confirms the four-coordinated geometry in solution. The free ligand and its respective homo- and heterobimetallic complexes were screened in vitro against a number of microorganisms to assess their biocidal properties. The biological activity data show that complexes exhibits significant antibacterial and antifungal activities as compared to ligand with few exceptions.     

Tiara[5]arenes: Synthesis,Solid‐State Conformational Studies,Host–Guest Properties,and Application as Nonporous Adaptive Crystals

Tiara[5]arenes (T[5]s), a new class of five‐fold symmetric oligophenolic macrocycles that are not accessible from the addition of formaldehyde to phenol, were synthesized for the first time. These pillar[5]arene‐derived structures display both unique conformational freedom, differing from that of pillararenes, with a rich blend of solid‐state conformations and excellent host–guest interactions in solution. Finally we show how this novel macrocyclic scaffold can be functionalized in a variety of ways and used as functional crystalline materials to distinguish uniquely between benzene and cyclohexane.     

Synthesis,Spectroscopy, Semi‐empirical and Biological Activities of Organotin(IV) Complexes with o‐Isopropyl Carbonodithioic Acid

New organotin(IV) complexes have been synthesized by treating potassium o‐isopropyl carbonodithioate with R₂SnCl₂/R₃SnCl in 1 : 2/1 : 1 M/L ratio. All complexes have been characterized by IR and NMR (¹H, ¹³C) spectroscopy. IR results shows that ligand acts as bidentate which is also confirmed by semi‐empirical study. NMR data reveals four coordinated geometry in solution. Computed positive heat of formation shows that complex 5 is thermodynamically unstable. UV/visible spectroscopy was used to assess the mode of interaction and binding of the complexes with DNA which shows that complex 5 exhibits higher binding constant as compared to complex 3 . In protein kinase inhibition assay, compound 3 was found most active, while other biological activities shows that triorganotin(IV) complexes are biologically more active as compared to diorganotin(IV) complexes.     

Complex dynamical invariant for a PT- symmetric Hamiltonian system in higher dimensions

With a view to get further insight into the integrability of a dynamical system, we investigate the complex invariant for a three-dimensional Hamiltonian system using the extended complex phase space approach (ECPSA) characterized by $x=x_1+i{p}_4,y=x_2+i{p}_5,z=x_3+i{p}_6,p_x=p_1+i{x}_4,p_y=p_2+i{x}_5$ and $p_z=p_3+i{x}_6$. For this purpose the rationalization method is utilized and the invariant obtained is expected to play an important role in the study of the complex trajectories for the system of concern.     

N-Heterocyclic carbene-mediated zwitterionic polymerization of N-substituted N-carboxyanhydrides toward poly(α-peptoid)s: kinetic, mechanism, and architectural control

N-Heterocyclic carbene (NHC)-mediated polymerizations of N-butyl N-carboxyanhydride (Bu-NCA) to produce cyclic poly(N-butyl glycine)s (c-NHC-PNBGs) have been investigated in various solvents with NHCs having differing steric and electronic properties. Control over the polymer molecular weight (MW) and polymerization rate is strongly dependent on the solvent and the NHC structure. Kinetic studies reveal that the propagating intermediates for the polymerization in low dielectric solvents (e.g., THF or toluene) maintain cyclic architectures with two chain ends in close contact through Coulombic interaction. The NHCs not only initiate the polymerization, but also mediate the chain propagation as intramolecular counterions. Side reactions are significantly suppressed in low dielectric solvents due to the reduced basicity and nucleophilicity of the negatively charged chain ends of the zwitterions, resulting in quasi-living polymerization behavior. By contrast, the two charged chain ends of the zwitterionic species are fully dissociated in high dielectric solvents. The chain propagation proceeds as in conventional anionic polymerizations, wherein side reactions (e.g., transamidation) compete with chain propagation, resulting in significantly diminished control over polymer MW. The cyclic zwitterionic propagating species can be converted into their linear polymeric analogues (l-NHC-PNBGs) by end-capping with electrophiles (e.g., acetyl chloride) or the NHC-free cyclic analogues (c-PNBGs) by treatment with NaN(TMS)(2), as evidenced by MALDI-TOF MS, NMR, and SEC analysis.     

Tiara[5]arenes: Synthesis,Solid-State Conformational Studies,Host–Guest Properties,and Application as Nonporous Adaptive Crystals

Tiara[5]arenes (T[5]s), a new class of five-fold symmetric oligophenolic macrocycles that are not accessible from the addition of formaldehyde to phenol, were synthesized for the first time. These pillar[5]arene-derived structures display both unique conformational freedom, differing from that of pillararenes, with a rich blend of solid-state conformations and excellent host–guest interactions in solution. Finally we show how this novel macrocyclic scaffold can be functionalized in a variety of ways and used as functional crystalline materials to distinguish uniquely between benzene and cyclohexane.     

Oxovanadium(IV) complexes with cephradine: Synthesis, Semi-Empirical study, spectroscopy, potentiometric study and antimicrobial activity

The reactions between cephradine and VOSO₄.3H₂O in 1:1, 1:2 and 1:3 molar ratios in methanol were investigated at room temperature, 0 °C and ?10 °C. In various pH conditions, the different complexes formulated as VO(H₂O)₃L^2?, VO(H₂O)L₂ ^2? and VL₃ ^? were formed by titration of VOSO₄.3H₂O and cephradine with NaOH. These complexes were characterized by elemental analysis and IR spectroscopy. IR spectra of all the complexes show the disappearance of ν(O-H) band of cephradine, which confirms complexation. Estimation of vanadium in the complexes was carried out by ICP-AES. The stability constants of each complex were calculated on the basis of which a general mechanism is hereby proposed with regard to the formation of these complexes. In complex (1) the cephradine ligand bind in bidentate [O,O] fashion together with a terminal oxo ligand and water molecules complete the metal coordination sphere. In complex (2) the cephradine ligands bind in bis-bidentate [O,O] fashion and the axial positions are occupied by the oxo ligand and a trans-water molecule. Biological screening tests show significant antibacterial and anti-fungal activities against various bacterial and fungal strains.