01920nas a2200253   4500008004100000022001400041245012200055210006900177260000900246300001600255490000700271520100100278653002201279653002601301653003001327653004001357653001501397100002701412700001501439700002301454700003101477700003001508856012801538       2020                        eng d  a1433-785100aPiezoelectric energy harvesting from a ferroelectric hybrid salt [Ph3MeP](4)[Ni(NCS)(6)] embedded in a polymer matrix0 aPiezoelectric energy harvesting from a ferroelectric hybrid salt  cJUN   a10368-103730 v593 a<p>Organic-inorganic hybrid ferroelectrics are an exciting class of molecular materials with promising applications in the area of energy and electronics. The synthesis, ferroelectric and piezoelectric energy harvesting behavior of a 3d metal ion-containing A(4)BX(6) type organic-inorganic hybrid salt [Ph3MeP](4)[Ni(NCS)(6)] (1) is now presented. P-E hysteresis loop studies on 1 show a remnant ferroelectric polarization value of 18.71 mu C cm(-2), at room temperature. Composite thermoplastic polyurethane (TPU) devices with 5, 10, 15 and 20 wt % compositions of 1 were prepared and employed for piezoelectric energy harvesting studies. A maximum output voltage of 19.29 V and a calculated power density value of 2.51 mW cm(-3) were observed for the 15 wt % 1-TPU device. The capacitor charging experiments on the 15 wt % 1-TPU composite device shows an excellent energy storage performance with the highest stored energies and measured charges of 198.8 mu J and 600 mu C, respectively.</p>
10aenergy conversion10amechanical properties10anon-covalent interactions10aorganic-inorganic hybrid composites10aPhosphorus1 aVijayakanth, Thangavel1 aRam, Farsa1 aPraveenkumar, Balu1 aShanmuganathan, Kadhiravan1 aBoomishankar, Ramamoorthy  uhttps://library.ncl.res.in/content/piezoelectric-energy-harvesting-ferroelectric-hybrid-salt-ph3mep4nincs6-embedded-polymer02236nas a2200181   4500008004100000022001400041245012100055210006900176260000800245300001600253490000700269520155800276100001601834700002201850700002401872700003001896856012801926       2025                        eng d  a0020-166900aPortal substituent modulations in chiral imido-Pd(II) cages for the enhanced separation of styrene oxide enantiomers0 aPortal substituent modulations in chiral imidoPdII cages for the  cMAY  a10313-103190 v643 a<p>
	Sensing and separation of enantiomers are crucial for the synthesis of biologically relevant compounds as well as for applications in catalysis and pharmaceutical development. Chiral coordination cages have gained significant attention as effective platforms for enantioselective processes through their well-defined, tunable cavities that facilitate host-guest interactions. In this study, we systematically explored the enantioselective binding and separation properties of two tetrahedral Pd(II) cages, 1-R and 2-R, with the molecular formula [Pd3(PO[N(RCH(CH3)Ph)3])4(C6O4X2)6] (X = Cl for 1-R, and X = F for 2-R). Their enantioselective abilities were investigated for small chiral molecules with diverse functional groups. Notably, the 2-R cage demonstrated a high enantioselectivity value of 88 for R-styrene oxide. Chiral separation experiments further revealed impressive enantiomeric excess (ee) values of 98% for R-styrene oxide from their racemic mixtures upon desorption from 2-R. The enhanced selectivity and separation efficiency were attributed to an optimal guest-to-cavity fit and the presence of multiple interaction sites within the host framework. Remarkably, portal substituent modulation in 2-R led to a 16-fold enhancement in enantioselective separation efficiency compared to 1-R, primarily due to improved portal dimensions, tighter molecular packing, and increased hydrogen bonding interactions. These findings highlight the potential of neutral chiral coordination cages for various enantioselective applications.</p>
1 aJose, Cavya1 aSarkar, Abhradeep1 aKhopade, Kishor, V.1 aBoomishankar, Ramamoorthy  uhttps://library.ncl.res.in/content/portal-substituent-modulations-chiral-imido-pdii-cages-enhanced-separation-styrene-oxide