A group of symmetrically‐trisubstituted‐1,3,5‐triazine‐based molecules have been studied extensively in order to create Piedfort pairs that are intended to be employed in sequestration of small molecules. Extensive inter and intramolecular interactions observed in the solid‐state of the studied triazine molecules lead to the formation of one‐dimensional ribbon and two‐dimensional sheet motifs. Koneramine formation was applied as a new strategy to increase the bulkiness of the substituents on 1,3,5‐triazine ring that prevented the formation of ribbons and sheets yet yielded hydrogen‐bonded dimer. The protonated forms of one of the triazine compound showed that the triazine ring nitrogens are more basic than amine nitrogens on the periphery; protonated N2,N4,N6‐triphenyl‐1,3,5‐triazine‐2,4,6‐triamine resulted in eccentric Piedfort pairs that displayed aesthetic structural patterns possessing variety of inter and intramolecular interactions including stacking between electron deficient triazine ring of one member and electron rich aryl ring of another member.
Unified statistics are valuable in the performance analysis of communication systems. In this context, Fox's Hfunction has been shown to be eminently suitable for diverse scenarios. Another pivotal requirement is to have a low computational complexity, which is often hard to achieve for generalized models. Given this motivation, in this article we have presented high-power, low-complexity solutions for the outage probability (OP) and the average symbol error probability (SEP). Additionally, diversity techniques are harnessed for mitigating the effect of fading, which are then analysed based on the results derived. The entire methodology is governed by the origin probability density function rather than approximating the performance metrics under high-power. All the presented mathematical expressions are compared and validated through computer simulations (Monte-Carlo) to verify the accuracy of the proposed framework.
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